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rs10830963 (MTNR1B)

What you carry at this position in your DNA and what research says about it.

Type 2 Diabetes Risk: 10/10 evidence, 93 publications.

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Sample genotype (not yours): C/C

Typical Diabetes Risk and Normal Blood Sugar

Typical blood sugar levels and a standard risk of metabolic conditions characterize this genotype.

What this genotype means: Typical fasting blood sugar levels; Standard risk of type 2 diabetes; Normal insulin secretion patterns.

Sample genotype (not yours): C/G

Moderately Increased Risk of Type 2 Diabetes

Slightly higher fasting blood sugar and a moderately increased risk of type 2 diabetes are associated with this genotype.

What this genotype means: Slightly elevated fasting blood sugar; Moderately increased risk of type 2 diabetes; Higher risk of gestational diabetes during pregnancy.

Sample genotype (not yours): G/G

Elevated Risk of Type 2 Diabetes

Higher fasting blood sugar and an increased risk of type 2 diabetes are associated with this genotype.

What this genotype means: Consistently higher fasting blood sugar; Increased risk of type 2 diabetes; Significantly higher risk of gestational diabetes.

About MTNR1B

Gene function and biological role

Gene Function: The MTNR1B gene encodes the melatonin receptor 1B, which is highly expressed in insulin-secreting beta cells of the pancreas [1]. Melatonin is a hormone primarily known for regulating sleep-wake cycles and circadian rhythms [2]. By binding to its receptors in the pancreas, melatonin helps coordinate the daily rhythms of insulin secretion [1]. Disruptions in this signaling pathway can impair the body's ability to manage blood sugar levels over time [2]. This makes the gene a critical link between sleep patterns, circadian biology, and metabolic health [1].

Variant Impact: The rs10830963 variant is an intron change in the MTNR1B gene that alters how the melatonin receptor is expressed in pancreatic cells [3]. Carrying the G allele increases the expression of these receptors, which paradoxically suppresses insulin release in response to glucose [4]. This reduction in insulin secretion leads to higher fasting blood sugar levels [5]. Over time, this mismatch in glucose regulation significantly raises the risk of developing metabolic conditions [6].

Key Insight: Melatonin, typically known as the sleep hormone, directly regulates insulin secretion in the pancreas, linking your sleep-wake cycle to blood sugar control.

Location: MTNR1B. Chromosome 11 · 11q14.3 · 93.0 Mb

Genotype Frequencies

Estimated prevalence by population

Global 60.5%; European 51.9%; African 86.8%; East Asian 32.1%; South Asian 34.4%; Americas 60.8%; Ashkenazi 58.6%; Finnish 41.8%; Middle Eastern 51.0%; Amish 28.2%.

Estimated CC genotype frequency.

Global 33.0%; European 40.3%; African 12.8%; East Asian 49.1%; South Asian 48.5%; Americas 34.4%; Ashkenazi 35.9%; Finnish 45.7%; Middle Eastern 40.8%; Amish 49.8%.

Estimated CG genotype frequency.

Global 6.5%; European 7.8%; African 0.5%; East Asian 18.8%; South Asian 17.1%; Americas 4.9%; Ashkenazi 5.5%; Finnish 12.5%; Middle Eastern 8.2%; Amish 22.0%.

Estimated GG genotype frequency.

Associated Traits

Showing effects for C/C genotype

Cardiovascular & Metabolic

Diabetes & Glycemic Traits

Type 2 Diabetes. Evidence: 10/10. Source: PMID 22885922. Typical Risk.

Fasting Glucose. Evidence: 10/10. Source: PMID 19060907. Typical Levels.

Insulin Secretion. Evidence: 7/10. Source: PMID 25524916. Typical Secretion.

HbA1c. Evidence: 10/10. Source: PMID 28898252. Typical Levels.

Endocrine & Reproductive

Pregnancy & Birth Complications

Gestational Diabetes. Evidence: 10/10. Source: PMID 35220425. Typical Risk.

Offspring Birth Weight. Evidence: 8/10. Source: PMID 27680694. Typical Weight.

Showing effects for C/G genotype

Type 2 Diabetes. Evidence: 10/10. Source: PMID 22885922. ~1.1x Higher Risk.

Fasting Glucose. Evidence: 10/10. Source: PMID 19060907. Slightly Elevated.

Insulin Secretion. Evidence: 7/10. Source: PMID 25524916. Slightly Reduced.

HbA1c. Evidence: 10/10. Source: PMID 28898252. Slightly Higher.

Gestational Diabetes. Evidence: 10/10. Source: PMID 35220425. ~1.4x Higher Risk.

Offspring Birth Weight. Evidence: 8/10. Source: PMID 27680694. Slightly Higher.

Showing effects for G/G genotype

Type 2 Diabetes. Evidence: 10/10. Source: PMID 22885922. ~1.2x Higher Risk.

Fasting Glucose. Evidence: 10/10. Source: PMID 19060907. Elevated.

Insulin Secretion. Evidence: 7/10. Source: PMID 25524916. Reduced Secretion.

HbA1c. Evidence: 10/10. Source: PMID 28898252. Higher Levels.

Offspring Birth Weight. Evidence: 8/10. Source: PMID 27680694. Higher Weight.

What CC Genotype Means

What this genotype means for the people who carry it

Sample genotype: CC (Homozygous)

Two copies of the C allele represent the baseline genetic profile for blood sugar regulation at this locus. Pancreatic beta cells maintain typical melatonin receptor levels, allowing for normal insulin release when blood sugar rises [1]. Consequently, fasting glucose levels and long-term HbA1c measurements remain within the typical range [2] [3]. The risk of developing type 2 diabetes or gestational diabetes during pregnancy is not elevated [4] [5]. Maintaining a balanced diet and regular exercise continues to support healthy metabolic function.

Typical fasting blood sugar levels; Standard risk of type 2 diabetes; Normal insulin secretion patterns.

What CG Genotype Means

Sample genotype: CG (Heterozygous)

One copy of the G allele alters melatonin receptor activity in the pancreas, which can mildly suppress insulin secretion [1]. This reduction in insulin release often leads to slightly elevated fasting blood sugar levels [2]. Long-term markers of glucose control, such as HbA1c, may also be slightly higher than average [3]. During pregnancy, this genetic variation increases the likelihood of developing gestational diabetes [4]. Managing carbohydrate intake and staying physically active are highly effective ways to offset this genetic predisposition.

Slightly elevated fasting blood sugar; Moderately increased risk of type 2 diabetes; Higher risk of gestational diabetes during pregnancy.

What GG Genotype Means

Sample genotype: GG (Homozygous)

Pancreatic beta cells with two G alleles express more melatonin receptors, which significantly dampens insulin secretion [1]. This blunted insulin response results in consistently higher fasting blood glucose levels [2]. Long-term blood sugar markers like HbA1c are typically elevated compared to those with other genotypes [3]. Pregnant individuals with this genotype face a notably higher risk of developing gestational diabetes [4].

Consistently higher fasting blood sugar; Increased risk of type 2 diabetes; Significantly higher risk of gestational diabetes.

Related Variants

Variants with shared genetic architecture

rs1387153 · MTNR1B Gene · Chr 11 · Blood Sugar Regulation

rs10830962 · MTNR1B Gene · Chr 11 · Gestational Diabetes Risk

rs4753426 · MTNR1B Gene · Chr 11 · Diabetes Risk

Sources

A central role for GRB10 in regulation of islet function in man.

Melatonin and the pathologies of weakened or dysregulated circadian oscillators.

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.

Common type 2 diabetes risk variant in MTNR1B worsens the deleterious effect of melatonin on glucose tolerance in humans.

Variants in MTNR1B influence fasting glucose levels.

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.

A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants.

Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.

Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes.

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Content updated August 2026.

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