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rs121912724

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121912724(G;G)
Make rs121912724(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116836361
GeneAPOA1
is asnp
is mentioned by
dbSNPrs121912724
ebirs121912724
HLIrs121912724
Exacrs121912724
Varsomers121912724
Maprs121912724
PheGenIrs121912724
hapmaprs121912724
1000 genomesrs121912724
hgdprs121912724
ensemblrs121912724
gopubmedrs121912724
geneviewrs121912724
scholarrs121912724
googlers121912724
pharmgkbrs121912724
gwascentralrs121912724
openSNPrs121912724
23andMers121912724
23andMe allrs121912724
SNP Nexus

SNPshotrs121912724
SNPdbers121912724
MSV3drs121912724
GWAS Ctlgrs121912724
Max Magnitude0
OMIM107680
Desc
Variant0016
Relatedalso
ClinVar
Risk rs121912724(G;G)
Alt rs121912724(G;G)
Reference rs121912724(T;T)
Significance Pathogenic
Disease Familial visceral amyloidosis
Variation info
Gene APOA1-AS APOA1
CLNDBN Familial visceral amyloidosis, Ostertag type
Reversed 1
HGVS NC_000011.9:g.116707077A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019516.27,



[PMID 24081495] Genetic Polymorphisms in the APOA1 Gene and their Relationship with Serum HDL Cholesterol Levels