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rs1401296

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;T)
Make rs1401296(C;C)
Make rs1401296(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position127431732
is asnp
is mentioned by
dbSNPrs1401296
ebirs1401296
HLIrs1401296
Exacrs1401296
Varsomers1401296
Maprs1401296
PheGenIrs1401296
hapmaprs1401296
1000 genomesrs1401296
hgdprs1401296
ensemblrs1401296
gopubmedrs1401296
geneviewrs1401296
scholarrs1401296
googlers1401296
pharmgkbrs1401296
gwascentralrs1401296
openSNPrs1401296
23andMers1401296
23andMe allrs1401296
SNP Nexus

SNPshotrs1401296
SNPdbers1401296
MSV3drs1401296
GWAS Ctlgrs1401296
GMAF0.3255
Max Magnitude
? (C;C) (C;T) (T;T) 28
linked to Cardiovascular Events

Several CVD risk variants were identified: In women, the combination of F5 rs7542281 × THBD rs1042580, together with three single F5 SNPs, was associated with CVD events. Among men, PROC rs1041296, when combined with either ICAM1 rs5030341 or F5 rs2269648, was associated with total mortality. As a single variant, PROC rs1401296, together with the F5 Leiden mutation, was associated with ischemic stroke events.[PMID 17677000OA-icon.png]