Have questions? Visit https://www.reddit.com/r/SNPedia

rs7542281

From SNPedia

Orientationplus
Stabilizedplus
Make rs7542281(C;C)
Make rs7542281(C;T)
Make rs7542281(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position169567201
GeneF5
is asnp
is mentioned by
dbSNPrs7542281
ebirs7542281
HLIrs7542281
Exacrs7542281
Varsomers7542281
Maprs7542281
PheGenIrs7542281
hapmaprs7542281
1000 genomesrs7542281
hgdprs7542281
ensemblrs7542281
gopubmedrs7542281
geneviewrs7542281
scholarrs7542281
googlers7542281
pharmgkbrs7542281
gwascentralrs7542281
openSNPrs7542281
23andMers7542281
23andMe allrs7542281
SNP Nexus

SNPshotrs7542281
SNPdbers7542281
MSV3drs7542281
GWAS Ctlgrs7542281
GMAF0.2342
Max Magnitude
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]


[PMID 18974842OA-icon.png] Gender differences in genetic risk profiles for cardiovascular disease.