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rs121909612

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909612(A;T)
Make rs121909612(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154585795
GeneFGA
is asnp
is mentioned by
dbSNPrs121909612
ebirs121909612
HLIrs121909612
Exacrs121909612
Varsomers121909612
Maprs121909612
PheGenIrs121909612
hapmaprs121909612
1000 genomesrs121909612
hgdprs121909612
ensemblrs121909612
gopubmedrs121909612
geneviewrs121909612
scholarrs121909612
googlers121909612
pharmgkbrs121909612
gwascentralrs121909612
openSNPrs121909612
23andMers121909612
23andMe allrs121909612
SNP Nexus

SNPshotrs121909612
SNPdbers121909612
MSV3drs121909612
GWAS Ctlgrs121909612
Max Magnitude0
OMIM134820
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121909612(T;T)
Alt rs121909612(T;T)
Reference rs121909612(A;A)
Significance Pathogenic
Disease Familial visceral amyloidosis
Variation info
Gene FGA
CLNDBN Familial visceral amyloidosis, Ostertag type
Reversed 1
HGVS NC_000004.11:g.155506947T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017871.29,