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rs3111754

From SNPedia

Orientationminus
Stabilizedminus
Make rs3111754(A;A)
Make rs3111754(A;G)
Make rs3111754(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position230868988
GeneITM2C
is asnp
is mentioned by
dbSNPrs3111754
ebirs3111754
HLIrs3111754
Exacrs3111754
Varsomers3111754
Maprs3111754
PheGenIrs3111754
hapmaprs3111754
1000 genomesrs3111754
hgdprs3111754
ensemblrs3111754
gopubmedrs3111754
geneviewrs3111754
scholarrs3111754
googlers3111754
pharmgkbrs3111754
gwascentralrs3111754
openSNPrs3111754
23andMers3111754
23andMe allrs3111754
SNP Nexus

SNPshotrs3111754
SNPdbers3111754
MSV3drs3111754
GWAS Ctlgrs3111754
GMAF0.45
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 20198315] Association of genetic variants with hemorrhagic stroke in Japanese individuals