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rs4775892

From SNPedia

Orientationplus
Stabilizedplus
Make rs4775892(G;G)
Make rs4775892(G;T)
Make rs4775892(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position50600917
GeneTRPM7
is asnp
is mentioned by
dbSNPrs4775892
ebirs4775892
HLIrs4775892
Exacrs4775892
Varsomers4775892
Maprs4775892
PheGenIrs4775892
hapmaprs4775892
1000 genomesrs4775892
hgdprs4775892
ensemblrs4775892
gopubmedrs4775892
geneviewrs4775892
scholarrs4775892
googlers4775892
pharmgkbrs4775892
gwascentralrs4775892
openSNPrs4775892
23andMers4775892
23andMe allrs4775892
SNP Nexus

SNPshotrs4775892
SNPdbers4775892
MSV3drs4775892
GWAS Ctlgrs4775892
GMAF0.1175
Max Magnitude
? (G;G) (G;T) (T;T) 28
[PMID 19644062OA-icon.png] Gene Variation of the Transient Receptor Potential Cation Channel, Subfamily M, Member 7 (TRPM7), and Risk of Incident Ischemic Stroke. Prospective, Nested, Case-Control Study