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rs121918389

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918389(C;T)
Make rs121918389(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position21012439
GeneAPOB
is asnp
is mentioned by
dbSNPrs121918389
ebirs121918389
HLIrs121918389
Exacrs121918389
Varsomers121918389
Maprs121918389
PheGenIrs121918389
hapmaprs121918389
1000 genomesrs121918389
hgdprs121918389
ensemblrs121918389
gopubmedrs121918389
geneviewrs121918389
scholarrs121918389
googlers121918389
pharmgkbrs121918389
gwascentralrs121918389
openSNPrs121918389
23andMers121918389
23andMe allrs121918389
SNP Nexus

SNPshotrs121918389
SNPdbers121918389
MSV3drs121918389
GWAS Ctlgrs121918389
Max Magnitude0
OMIM107730
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121918389(T;T)
Alt rs121918389(T;T)
Reference rs121918389(C;C)
Significance Pathogenic
Disease Familial hypobetalipoproteinemia
Variation info
Gene APOB
CLNDBN Familial hypobetalipoproteinemia
Reversed 1
HGVS NC_000002.11:g.21235311G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019483.25,