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rs121918155

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918155(C;C)
Make rs121918155(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position127426227
GenePROC
is asnp
is mentioned by
dbSNPrs121918155
ebirs121918155
HLIrs121918155
Exacrs121918155
Varsomers121918155
Maprs121918155
PheGenIrs121918155
hapmaprs121918155
1000 genomesrs121918155
hgdprs121918155
ensemblrs121918155
gopubmedrs121918155
geneviewrs121918155
scholarrs121918155
googlers121918155
pharmgkbrs121918155
gwascentralrs121918155
openSNPrs121918155
23andMers121918155
23andMe allrs121918155
SNP Nexus

SNPshotrs121918155
SNPdbers121918155
MSV3drs121918155
GWAS Ctlgrs121918155
Max Magnitude0
OMIM612283
Desc
Variant0019
Relatedalso
ClinVar
Risk rs121918155(C;C)
Alt rs121918155(C;C)
Reference rs121918155(G;G)
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.128183803G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000000709.3,