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rs121918157

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918157(C;G)
Make rs121918157(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position127428895
GenePROC
is asnp
is mentioned by
dbSNPrs121918157
ebirs121918157
HLIrs121918157
Exacrs121918157
Varsomers121918157
Maprs121918157
PheGenIrs121918157
hapmaprs121918157
1000 genomesrs121918157
hgdprs121918157
ensemblrs121918157
gopubmedrs121918157
geneviewrs121918157
scholarrs121918157
googlers121918157
pharmgkbrs121918157
gwascentralrs121918157
openSNPrs121918157
23andMers121918157
23andMe allrs121918157
SNP Nexus

SNPshotrs121918157
SNPdbers121918157
MSV3drs121918157
GWAS Ctlgrs121918157
Max Magnitude0
OMIM612283
Desc
Variant0021
Relatedalso
ClinVar
Risk rs121918157(G;G)
Alt rs121918157(G;G)
Reference rs121918157(C;C)
Significance Pathogenic
Disease Thrombophilia
Variation info
Gene PROC
CLNDBN Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive
Reversed 0
HGVS NC_000002.11:g.128186471C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000711.4,