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rs2269648

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs2269648(C;T)
Make rs2269648(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position169586812
GeneF5
is asnp
is mentioned by
dbSNPrs2269648
ebirs2269648
HLIrs2269648
Exacrs2269648
Varsomers2269648
Maprs2269648
PheGenIrs2269648
hapmaprs2269648
1000 genomesrs2269648
hgdprs2269648
ensemblrs2269648
gopubmedrs2269648
geneviewrs2269648
scholarrs2269648
googlers2269648
pharmgkbrs2269648
gwascentralrs2269648
openSNPrs2269648
23andMers2269648
23andMe allrs2269648
SNP Nexus

SNPshotrs2269648
SNPdbers2269648
MSV3drs2269648
GWAS Ctlgrs2269648
GMAF0.3939
Max Magnitude0
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.


[PMID 26054681] Association of seven thrombotic pathway gene CpG-SNPs with coronary heart disease