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rs121918156

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918156(C;T)
Make rs121918156(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position127427219
GenePROC
is asnp
is mentioned by
dbSNPrs121918156
ebirs121918156
HLIrs121918156
Exacrs121918156
Varsomers121918156
Maprs121918156
PheGenIrs121918156
hapmaprs121918156
1000 genomesrs121918156
hgdprs121918156
ensemblrs121918156
gopubmedrs121918156
geneviewrs121918156
scholarrs121918156
googlers121918156
pharmgkbrs121918156
gwascentralrs121918156
openSNPrs121918156
23andMers121918156
23andMe allrs121918156
SNP Nexus

SNPshotrs121918156
SNPdbers121918156
MSV3drs121918156
GWAS Ctlgrs121918156
Max Magnitude0
OMIM612283
Desc
Variant0020
Relatedalso
ClinVar
Risk rs121918156(T;T)
Alt rs121918156(T;T)
Reference rs121918156(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.128184795C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000710.3,