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rs121918141

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918141(C;T)
Make rs121918141(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position127428602
GenePROC
is asnp
is mentioned by
dbSNPrs121918141
ebirs121918141
HLIrs121918141
Exacrs121918141
Varsomers121918141
Maprs121918141
PheGenIrs121918141
hapmaprs121918141
1000 genomesrs121918141
hgdprs121918141
ensemblrs121918141
gopubmedrs121918141
geneviewrs121918141
scholarrs121918141
googlers121918141
pharmgkbrs121918141
gwascentralrs121918141
openSNPrs121918141
23andMers121918141
23andMe allrs121918141
SNP Nexus

SNPshotrs121918141
SNPdbers121918141
MSV3drs121918141
GWAS Ctlgrs121918141
Max Magnitude0
OMIM612283
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918141(T;T)
Alt rs121918141(T;T)
Reference rs121918141(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.128186178C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000690.3,