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rs1799810

From SNPedia

Orientationplus
Stabilizedplus
Make rs1799810(A;A)
Make rs1799810(A;T)
Make rs1799810(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position127418464
GenePROC
is asnp
is mentioned by
dbSNPrs1799810
ebirs1799810
HLIrs1799810
Exacrs1799810
Varsomers1799810
Maprs1799810
PheGenIrs1799810
hapmaprs1799810
1000 genomesrs1799810
hgdprs1799810
ensemblrs1799810
gopubmedrs1799810
geneviewrs1799810
scholarrs1799810
googlers1799810
pharmgkbrs1799810
gwascentralrs1799810
openSNPrs1799810
23andMers1799810
23andMe allrs1799810
SNP Nexus

SNPshotrs1799810
SNPdbers1799810
MSV3drs1799810
GWAS Ctlgrs1799810
GMAF0.3494
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 20707712OA-icon.png]
Trait
Title A genome-wide association study of self-rated health
Risk Allele T
P-val 0.000009
Odds Ratio 0.02 [NR] unit decrease


[PMID 20031567OA-icon.png] An evaluation of candidate genes of inflammation and thrombosis in relation to the risk of venous thromboembolism: The Women's Genome Health Study.


[PMID 24300144] [Phenotypic detection and structure analysis of a PC missense mutation (Met406Ile) resulted in venous thromboembolism]