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rs121918154

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918154(C;T)
Make rs121918154(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position127428374
GenePROC
is asnp
is mentioned by
dbSNPrs121918154
ebirs121918154
HLIrs121918154
Exacrs121918154
Varsomers121918154
Maprs121918154
PheGenIrs121918154
hapmaprs121918154
1000 genomesrs121918154
hgdprs121918154
ensemblrs121918154
gopubmedrs121918154
geneviewrs121918154
scholarrs121918154
googlers121918154
pharmgkbrs121918154
gwascentralrs121918154
openSNPrs121918154
23andMers121918154
23andMe allrs121918154
SNP Nexus

SNPshotrs121918154
SNPdbers121918154
MSV3drs121918154
GWAS Ctlgrs121918154
Max Magnitude0
OMIM612283
Desc
Variant0016
Relatedalso
ClinVar
Risk rs121918154(T;T)
Alt rs121918154(T;T)
Reference rs121918154(C;C)
Significance Pathogenic
Disease Thrombophilia
Variation info
Gene PROC
CLNDBN Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.128185950C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000706.3,