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

rs5935

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs5935(C;T)
Make rs5935(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position127428451
GenePROC
is asnp
is mentioned by
dbSNPrs5935
ebirs5935
HLIrs5935
Exacrs5935
Varsomers5935
Maprs5935
PheGenIrs5935
hapmaprs5935
1000 genomesrs5935
hgdprs5935
ensemblrs5935
gopubmedrs5935
geneviewrs5935
scholarrs5935
googlers5935
pharmgkbrs5935
gwascentralrs5935
openSNPrs5935
23andMers5935
23andMe allrs5935
SNP Nexus

SNPshotrs5935
SNPdbers5935
MSV3drs5935
GWAS Ctlgrs5935
GMAF0.01423
Max Magnitude0
ClinVar
Risk rs5935(T;T)
Alt rs5935(T;T)
Reference rs5935(C;C)
Significance Non-pathogenic
Disease Thrombophilia
Variation info
Gene PROC
CLNDBN Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.128186027C>T
CLNSRC
CLNACC RCV000233040.1,


[PMID 17048007OA-icon.png] Association of warfarin dose with genes involved in its action and metabolism.