rs10906115

Orientation

plus

Stabilized

plus

Make rs10906115(A;A)

Make rs10906115(A;G)

Make rs10906115(G;G)

Reference

GRCh38 38.1/142

Chromosome

10

Position

12272998

is a	snp
is	mentioned by
dbSNP	rs10906115
dbSNP (classic)	rs10906115
ClinGen	rs10906115
ebi	rs10906115
HLI	rs10906115
Exac	rs10906115
Gnomad	rs10906115
Varsome	rs10906115
LitVar	rs10906115
Map	rs10906115
PheGenI	rs10906115
Biobank	rs10906115
1000 genomes	rs10906115
hgdp	rs10906115
ensembl	rs10906115
geneview	rs10906115
scholar	rs10906115
google	rs10906115
pharmgkb	rs10906115
gwascentral	rs10906115
openSNP	rs10906115
23andMe	rs10906115
SNPshot	rs10906115
SNPdbe	rs10906115
MSV3d	rs10906115
GWAS Ctlg	rs10906115

GMAF

0.3655

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 20862305]
Trait
Title	Identification of new genetic risk variants for type 2 diabetes
Risk Allele	A
P-val	1E-8
Odds Ratio	1.13 [1.08-1.18]

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