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rs121918151

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918151(C;T)
Make rs121918151(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position127428426
GenePROC
is asnp
is mentioned by
dbSNPrs121918151
ebirs121918151
HLIrs121918151
Exacrs121918151
Varsomers121918151
Maprs121918151
PheGenIrs121918151
hapmaprs121918151
1000 genomesrs121918151
hgdprs121918151
ensemblrs121918151
gopubmedrs121918151
geneviewrs121918151
scholarrs121918151
googlers121918151
pharmgkbrs121918151
gwascentralrs121918151
openSNPrs121918151
23andMers121918151
23andMe allrs121918151
SNP Nexus

SNPshotrs121918151
SNPdbers121918151
MSV3drs121918151
GWAS Ctlgrs121918151
Max Magnitude0
OMIM612283
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121918151(T;T)
Alt rs121918151(T;T)
Reference rs121918151(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.128186002C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000702.3,