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rs121918149

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918149(A;A)
Make rs121918149(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position127421438
GenePROC
is asnp
is mentioned by
dbSNPrs121918149
ebirs121918149
HLIrs121918149
Exacrs121918149
Varsomers121918149
Maprs121918149
PheGenIrs121918149
hapmaprs121918149
1000 genomesrs121918149
hgdprs121918149
ensemblrs121918149
gopubmedrs121918149
geneviewrs121918149
scholarrs121918149
googlers121918149
pharmgkbrs121918149
gwascentralrs121918149
openSNPrs121918149
23andMers121918149
23andMe allrs121918149
SNP Nexus

SNPshotrs121918149
SNPdbers121918149
MSV3drs121918149
GWAS Ctlgrs121918149
Max Magnitude0
OMIM612283
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121918149(A;A)
Alt rs121918149(A;A)
Reference rs121918149(G;G)
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.128179014G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000700.4,