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rs121912726

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121912726(C;C)
Make rs121912726(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116836392
GeneAPOA1
is asnp
is mentioned by
dbSNPrs121912726
ebirs121912726
HLIrs121912726
Exacrs121912726
Varsomers121912726
Maprs121912726
PheGenIrs121912726
hapmaprs121912726
1000 genomesrs121912726
hgdprs121912726
ensemblrs121912726
gopubmedrs121912726
geneviewrs121912726
scholarrs121912726
googlers121912726
pharmgkbrs121912726
gwascentralrs121912726
openSNPrs121912726
23andMers121912726
23andMe allrs121912726
SNP Nexus

SNPshotrs121912726
SNPdbers121912726
MSV3drs121912726
GWAS Ctlgrs121912726
Max Magnitude0
OMIM107680
Desc
Variant0021
Relatedalso
ClinVar
Risk rs121912726(C;C)
Alt rs121912726(C;C)
Reference rs121912726(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.116707108A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019521.27,