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rs121918160

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918160(C;T)
Make rs121918160(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position127428495
GenePROC
is asnp
is mentioned by
dbSNPrs121918160
ebirs121918160
HLIrs121918160
Exacrs121918160
Varsomers121918160
Maprs121918160
PheGenIrs121918160
hapmaprs121918160
1000 genomesrs121918160
hgdprs121918160
ensemblrs121918160
gopubmedrs121918160
geneviewrs121918160
scholarrs121918160
googlers121918160
pharmgkbrs121918160
gwascentralrs121918160
openSNPrs121918160
23andMers121918160
23andMe allrs121918160
SNP Nexus

SNPshotrs121918160
SNPdbers121918160
MSV3drs121918160
GWAS Ctlgrs121918160
Max Magnitude0
OMIM612283
Desc
Variant0025
Relatedalso
OMIM176860
Desc
Variant
Relatedalso
ClinVar
Risk rs121918160(T;T)
Alt rs121918160(T;T)
Reference rs121918160(C;C)
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.128186071C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000715.3,