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rs121912729

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121912729(C;C)
Make rs121912729(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116836019
GeneAPOA1
is asnp
is mentioned by
dbSNPrs121912729
ebirs121912729
HLIrs121912729
Exacrs121912729
Varsomers121912729
Maprs121912729
PheGenIrs121912729
hapmaprs121912729
1000 genomesrs121912729
hgdprs121912729
ensemblrs121912729
gopubmedrs121912729
geneviewrs121912729
scholarrs121912729
googlers121912729
pharmgkbrs121912729
gwascentralrs121912729
openSNPrs121912729
23andMers121912729
23andMe allrs121912729
SNP Nexus

SNPshotrs121912729
SNPdbers121912729
MSV3drs121912729
GWAS Ctlgrs121912729
Max Magnitude0
OMIM107680
Desc
Variant0026
Relatedalso
ClinVar
Risk rs121912729(C;C)
Alt rs121912729(C;C)
Reference rs121912729(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.116706735A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019526.27,