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rs121912723

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912723(C;T)
Make rs121912723(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116836290
GeneAPOA1
is asnp
is mentioned by
dbSNPrs121912723
ebirs121912723
HLIrs121912723
Exacrs121912723
Varsomers121912723
Maprs121912723
PheGenIrs121912723
hapmaprs121912723
1000 genomesrs121912723
hgdprs121912723
ensemblrs121912723
gopubmedrs121912723
geneviewrs121912723
scholarrs121912723
googlers121912723
pharmgkbrs121912723
gwascentralrs121912723
openSNPrs121912723
23andMers121912723
23andMe allrs121912723
SNP Nexus

SNPshotrs121912723
SNPdbers121912723
MSV3drs121912723
GWAS Ctlgrs121912723
Max Magnitude0
OMIM107680
Desc
Variant0015
Relatedalso
ClinVar
Risk rs121912723(T;T)
Alt rs121912723(T;T)
Reference rs121912723(C;C)
Significance Pathogenic
Disease Apolipoprotein A-I deficiency
Variation info
Gene APOA1-AS APOA1
CLNDBN Apolipoprotein A-I deficiency
Reversed 1
HGVS NC_000011.9:g.116707006G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019515.27,