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rs5030341

From SNPedia

Orientationplus
Stabilizedplus
Make rs5030341(-;-)
Make rs5030341(-;CT)
Make rs5030341(CT;CT)
ReferenceGRCh38 38.1/141
Chromosome19
Position10272597
GeneICAM1
is asnp
is mentioned by
dbSNPrs5030341
ebirs5030341
HLIrs5030341
Exacrs5030341
Varsomers5030341
Maprs5030341
PheGenIrs5030341
hapmaprs5030341
1000 genomesrs5030341
hgdprs5030341
ensemblrs5030341
gopubmedrs5030341
geneviewrs5030341
scholarrs5030341
googlers5030341
pharmgkbrs5030341
gwascentralrs5030341
openSNPrs5030341
23andMers5030341
23andMe allrs5030341
SNP Nexus

SNPshotrs5030341
SNPdbers5030341
MSV3drs5030341
GWAS Ctlgrs5030341
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]