rs10830962

Orientation

plus

Stabilized

plus

Make rs10830962(C;C)

Make rs10830962(C;G)

Make rs10830962(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

92965261

is a	snp
is	mentioned by
dbSNP	rs10830962
dbSNP (classic)	rs10830962
ClinGen	rs10830962
ebi	rs10830962
HLI	rs10830962
Exac	rs10830962
Gnomad	rs10830962
Varsome	rs10830962
LitVar	rs10830962
Map	rs10830962
PheGenI	rs10830962
Biobank	rs10830962
1000 genomes	rs10830962
hgdp	rs10830962
ensembl	rs10830962
geneview	rs10830962
scholar	rs10830962
google	rs10830962
pharmgkb	rs10830962
gwascentral	rs10830962
openSNP	rs10830962
23andMe	rs10830962
SNPshot	rs10830962
SNPdbe	rs10830962
MSV3d	rs10830962
GWAS Ctlg	rs10830962

GMAF

0.4917

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

[PMID 19088850] rs10830962, rs4753426, and rs10830963 were significantly associated with higher fasting plasma glucose concentrations and reduced OGTT- and IVGTT-induced insulin release. rs3781638 displayed significant association with lower fasting plasma glucose levels and increased OGTT-induced insulin release

[PMID 22233651] A Genome-Wide Association Study of Gestational Diabetes Mellitus in Korean Women

GWAS snp
PMID	[PMID 21909109]
Trait
Title	Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits.
Risk Allele	C
P-val	1E-16
Odds Ratio	0.0445 [0.034-0.055] mg/dL increase

GWAS snp
PMID	[PMID 22399527]
Trait
Title	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.
Risk Allele	G
P-val	5E-16
Odds Ratio	0.1200 None

[PMID 19184136] Examination of association of genes in the serotonin system to autism.

[PMID 20959387] Association of rs10830963 and rs10830962 SNPs in the melatonin receptor (MTNR1B) gene among Han Chinese women with polycystic ovary syndrome.

GWAS snp
PMID	[PMID 23575436]
Trait	Glycemic traits
Title	New susceptibility loci in MYL2, C12orf51 and OAS1 associated with 1-h plasma glucose as predisposing risk factors for type 2 diabetes in the Korean population.
Risk Allele	C
P-val	5E-13
Odds Ratio	.04 [0.029-0.053] mmol-1 increase

[PMID 24157813] Association between Genetic Variations in MTNR1A and MTNR1B Genes and Gestational Diabetes Mellitus in Han Chinese Women

[PMID 23611530] Genetics of melatonin receptor type 2 is associated with left ventricular function in hypertensive patients treated according to guidelines.