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rs146922325

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146922325(C;T)
Make rs146922325(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position127426114
GenePROC
is asnp
is mentioned by
dbSNPrs146922325
ebirs146922325
HLIrs146922325
Exacrs146922325
Varsomers146922325
Maprs146922325
PheGenIrs146922325
hapmaprs146922325
1000 genomesrs146922325
hgdprs146922325
ensemblrs146922325
gopubmedrs146922325
geneviewrs146922325
scholarrs146922325
googlers146922325
pharmgkbrs146922325
gwascentralrs146922325
openSNPrs146922325
23andMers146922325
23andMe allrs146922325
SNP Nexus

SNPshotrs146922325
SNPdbers146922325
MSV3drs146922325
GWAS Ctlgrs146922325
GMAF0.001837
Max Magnitude0
ClinVar
Risk rs146922325(T;T)
Alt rs146922325(T;T)
Reference rs146922325(C;C)
Significance Probable-Pathogenic
Disease Thrombophilia
Variation info
Gene PROC
CLNDBN Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.128183690C>T
CLNSRC ClinVar University of Washington
CLNACC RCV000148748.1,