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rs1436955

From SNPedia

Orientationminus
Stabilizedminus
Make rs1436955(A;A)
Make rs1436955(A;G)
Make rs1436955(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position62112183
is asnp
is mentioned by
dbSNPrs1436955
ebirs1436955
HLIrs1436955
Exacrs1436955
Varsomers1436955
Maprs1436955
PheGenIrs1436955
hapmaprs1436955
1000 genomesrs1436955
hgdprs1436955
ensemblrs1436955
gopubmedrs1436955
geneviewrs1436955
scholarrs1436955
googlers1436955
pharmgkbrs1436955
gwascentralrs1436955
openSNPrs1436955
23andMers1436955
23andMe allrs1436955
SNP Nexus

SNPshotrs1436955
SNPdbers1436955
MSV3drs1436955
GWAS Ctlgrs1436955
GMAF0.3035
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20862305OA-icon.png]
Trait
Title Identification of new genetic risk variants for type 2 diabetes
Risk Allele C
P-val 7E-7
Odds Ratio 1.13 [1.08-1.19]


[PMID 21909839] Genetic variants at CDC123/CAMK1D and SPRY2 are associated with susceptibility to type 2 diabetes in the Japanese population.