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

rs6122

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs6122(C;T)
Make rs6122(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position93927251
GenePROS1
is asnp
is mentioned by
dbSNPrs6122
ebirs6122
HLIrs6122
Exacrs6122
Varsomers6122
Maprs6122
PheGenIrs6122
hapmaprs6122
1000 genomesrs6122
hgdprs6122
ensemblrs6122
gopubmedrs6122
geneviewrs6122
scholarrs6122
googlers6122
pharmgkbrs6122
gwascentralrs6122
openSNPrs6122
23andMers6122
23andMe allrs6122
SNP Nexus

SNPshotrs6122
SNPdbers6122
MSV3drs6122
GWAS Ctlgrs6122
Max Magnitude0
ClinVar
Risk rs6122(T;T)
Alt rs6122(T;T)
Reference rs6122(C;C)
Significance Probable-Pathogenic
Disease Thrombophilia due to protein S deficiency
Variation info
Gene PROS1
CLNDBN Thrombophilia due to protein S deficiency, autosomal recessive
Reversed 1
HGVS NC_000003.11:g.93646095G>A
CLNSRC
CLNACC RCV000197958.1,