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rs121918158

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918158(A;A)
Make rs121918158(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position127428575
GenePROC
is asnp
is mentioned by
dbSNPrs121918158
ebirs121918158
HLIrs121918158
Exacrs121918158
Varsomers121918158
Maprs121918158
PheGenIrs121918158
hapmaprs121918158
1000 genomesrs121918158
hgdprs121918158
ensemblrs121918158
gopubmedrs121918158
geneviewrs121918158
scholarrs121918158
googlers121918158
pharmgkbrs121918158
gwascentralrs121918158
openSNPrs121918158
23andMers121918158
23andMe allrs121918158
SNP Nexus

SNPshotrs121918158
SNPdbers121918158
MSV3drs121918158
GWAS Ctlgrs121918158
Max Magnitude0
OMIM612283
Desc
Variant0022
Relatedalso
ClinVar
Risk rs121918158(A;A)
Alt rs121918158(A;A)
Reference rs121918158(G;G)
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.128186151G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000712.3,