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rs3792267

From SNPedia

Orientationplus
Stabilizedplus
Make rs3792267(A;A)
Make rs3792267(A;G)
Make rs3792267(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240591757
GeneCAPN10
is asnp
is mentioned by
dbSNPrs3792267
ebirs3792267
HLIrs3792267
Exacrs3792267
Varsomers3792267
Maprs3792267
PheGenIrs3792267
hapmaprs3792267
1000 genomesrs3792267
hgdprs3792267
ensemblrs3792267
gopubmedrs3792267
geneviewrs3792267
scholarrs3792267
googlers3792267
pharmgkbrs3792267
gwascentralrs3792267
openSNPrs3792267
23andMers3792267
23andMe allrs3792267
SNP Nexus

SNPshotrs3792267
SNPdbers3792267
MSV3drs3792267
GWAS Ctlgrs3792267
GMAF0.1993
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 16857402] summary, indicating a small effect of this SNP, seen only in meta-analyses

rs3792267 associated with noninsulin-dependent diabetes mellitus, polycystic ovary syndrome, type 2 diabetes, gestational diabetes and obesity

OMIM605286
DescCALPAIN 10; CAPN10
Variant
Relatedalso

[PMID 19752882] Association of calpain-10 gene polymorphism and posttransplant diabetes mellitus in kidney transplant patients medicated with tacrolimus


[PMID 20178008OA-icon.png] Association of Diabetes Susceptibility Gene Calpain-10 with Pancreatic Cancer Among Smokers


[PMID 20470430OA-icon.png] Common polymorphisms of calpain-10 and the risk of Type 2 Diabetes in a Tunisian Arab population: a case-control study

OMIM605286
Desc
Variant0001
Relatedalso
[PMID 14730479OA-icon.png] Are variants in the CAPN10 gene related to risk of type 2 diabetes? A quantitative assessment of population and family-based association studies.


[PMID 15371359OA-icon.png] Testing for Hardy-Weinberg equilibrium in samples with related individuals.


[PMID 17570749OA-icon.png] Genetic prediction of future type 2 diabetes.


[PMID 17825092OA-icon.png] Genetic association of glutathione peroxidase-1 with coronary artery calcification in type 2 diabetes: a case control study with multi-slice computed tomography.


[PMID 18599530OA-icon.png] Ser1369Ala variant in sulfonylurea receptor gene ABCC8 is associated with antidiabetic efficacy of gliclazide in Chinese type 2 diabetic patients.


[PMID 18603647OA-icon.png] Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response.


[PMID 18936436OA-icon.png] Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994.


[PMID 19193380OA-icon.png] Replication of calpain-10 genetic association with carotid intima-media thickness.


[PMID 19387820OA-icon.png] Genetic polymorphisms of FSHR, CYP17, CYP1A1, CAPN10, INSR, SERPINE1 genes in adolescent girls with polycystic ovary syndrome.


[PMID 19643578OA-icon.png] Genetic risk factors for type 2 diabetes with pharmacologic intervention in African-American patients with schizophrenia or schizoaffective disorder.


[PMID 20075150OA-icon.png] Utility of genetic and non-genetic risk factors in prediction of type 2 diabetes: Whitehall II prospective cohort study.


[PMID 20119856] Haplotype association of calpain 10 gene variants with type 2 diabetes mellitus in an Irish sample.


[PMID 20142250OA-icon.png] Diabetes genes and prostate cancer in the Atherosclerosis Risk in Communities study.


[PMID 20667559] Association of calpain 10 gene polymorphisms with type 2 diabetes mellitus in Southern Indians.


[PMID 21278902OA-icon.png] Genetic risk profiling for prediction of type 2 diabetes.


[PMID 21834909] A replication study of the IRS1, CAPN10, TCF7L2, and PPARG gene polymorphisms associated with type 2 diabetes in two different populations of Mexico.


[PMID 22391941] Meta-analysis of association studies between five candidate genes and type 2 diabetes in Chinese Han population.


[PMID 24612564] Association of IRS-1, CAPN10 and PPARG gene polymorphisms with T2DM in the high risk population of Hyderabad, India


ClinVar
Risk rs3792267(A;A)
Alt rs3792267(A;A)
Reference rs3792267(G;G)
Significance Other
Disease Diabetes mellitus type 2
Variation info
Gene CAPN10
CLNDBN Diabetes mellitus type 2
Reversed 0
HGVS NC_000002.11:g.241531174G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005398.2,