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rs121918145

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918145(C;T)
Make rs121918145(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position127426178
GenePROC
is asnp
is mentioned by
dbSNPrs121918145
ebirs121918145
HLIrs121918145
Exacrs121918145
Varsomers121918145
Maprs121918145
PheGenIrs121918145
hapmaprs121918145
1000 genomesrs121918145
hgdprs121918145
ensemblrs121918145
gopubmedrs121918145
geneviewrs121918145
scholarrs121918145
googlers121918145
pharmgkbrs121918145
gwascentralrs121918145
openSNPrs121918145
23andMers121918145
23andMe allrs121918145
SNP Nexus

SNPshotrs121918145
SNPdbers121918145
MSV3drs121918145
GWAS Ctlgrs121918145
Max Magnitude0
OMIM612283
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121918145(T;T)
Alt rs121918145(T;T)
Reference rs121918145(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.128183754C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000696.3,