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rs121918148

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918148(A;C)
Make rs121918148(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position127421397
GenePROC
is asnp
is mentioned by
dbSNPrs121918148
ebirs121918148
HLIrs121918148
Exacrs121918148
Varsomers121918148
Maprs121918148
PheGenIrs121918148
hapmaprs121918148
1000 genomesrs121918148
hgdprs121918148
ensemblrs121918148
gopubmedrs121918148
geneviewrs121918148
scholarrs121918148
googlers121918148
pharmgkbrs121918148
gwascentralrs121918148
openSNPrs121918148
23andMers121918148
23andMe allrs121918148
SNP Nexus

SNPshotrs121918148
SNPdbers121918148
MSV3drs121918148
GWAS Ctlgrs121918148
Max Magnitude0
OMIM612283
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121918148(C;C)
Alt rs121918148(C;C)
Reference rs121918148(A;A)
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.128178973A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000000699.4,