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rs670659

From SNPedia

Orientationplus
Stabilizedplus
Make rs670659(C;C)
Make rs670659(C;T)
Make rs670659(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position240998475
GeneRGS7
is asnp
is mentioned by
dbSNPrs670659
ebirs670659
HLIrs670659
Exacrs670659
Varsomers670659
Maprs670659
PheGenIrs670659
hapmaprs670659
1000 genomesrs670659
hgdprs670659
ensemblrs670659
gopubmedrs670659
geneviewrs670659
scholarrs670659
googlers670659
pharmgkbrs670659
gwascentralrs670659
openSNPrs670659
23andMers670659
23andMe allrs670659
SNP Nexus

SNPshotrs670659
SNPdbers670659
MSV3drs670659
GWAS Ctlgrs670659
GMAF0.3365
Max Magnitude
? (C;C) (C;T) (T;T) 28
Gene variants associated with deep vein thrombosis.[PMID 18349091]

Updated analysis of gene variants associated with deep vein thrombosis.[PMID 20124536]


[PMID 21232005OA-icon.png] New gene variants associated with venous thrombosis: a replication study in White and Black Americans.