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rs1041296

From SNPedia

Orientationminus
Stabilizedminus
Make rs1041296(C;C)
Make rs1041296(C;T)
Make rs1041296(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position130204767
is asnp
is mentioned by
dbSNPrs1041296
ebirs1041296
HLIrs1041296
Exacrs1041296
Varsomers1041296
Maprs1041296
PheGenIrs1041296
hapmaprs1041296
1000 genomesrs1041296
hgdprs1041296
ensemblrs1041296
gopubmedrs1041296
geneviewrs1041296
scholarrs1041296
googlers1041296
pharmgkbrs1041296
gwascentralrs1041296
openSNPrs1041296
23andMers1041296
23andMe allrs1041296
SNP Nexus

SNPshotrs1041296
SNPdbers1041296
MSV3drs1041296
GWAS Ctlgrs1041296
GMAF0.1685
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]

NOTE: SNPedia has raised a question with the authors of this paper ([PMID 17677000OA-icon.png]), in that it appears that their mention of "rs1041296" is a typographical error, when they intended to refer to SNP rs1401296. Once a response is received from the authors, we will update the associated entries, and until then, Caveat Emptor.