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rs121918146

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918146(A;A)
Make rs121918146(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position127428485
GenePROC
is asnp
is mentioned by
dbSNPrs121918146
ebirs121918146
HLIrs121918146
Exacrs121918146
Varsomers121918146
Maprs121918146
PheGenIrs121918146
hapmaprs121918146
1000 genomesrs121918146
hgdprs121918146
ensemblrs121918146
gopubmedrs121918146
geneviewrs121918146
scholarrs121918146
googlers121918146
pharmgkbrs121918146
gwascentralrs121918146
openSNPrs121918146
23andMers121918146
23andMe allrs121918146
SNP Nexus

SNPshotrs121918146
SNPdbers121918146
MSV3drs121918146
GWAS Ctlgrs121918146
Max Magnitude0
OMIM612283
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121918146(A;A)
Alt rs121918146(A;A)
Reference rs121918146(G;G)
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.128186061G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000697.3,