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rs587777761

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777761(-;-)
Make rs587777761(-;A)
ReferenceGRCh38 38.1/142
Chromosome4
Position154585807
GeneFGA
is asnp
is mentioned by
dbSNPrs587777761
ebirs587777761
HLIrs587777761
Exacrs587777761
Varsomers587777761
Maprs587777761
PheGenIrs587777761
hapmaprs587777761
1000 genomesrs587777761
hgdprs587777761
ensemblrs587777761
gopubmedrs587777761
geneviewrs587777761
scholarrs587777761
googlers587777761
pharmgkbrs587777761
gwascentralrs587777761
openSNPrs587777761
23andMers587777761
23andMe allrs587777761
SNP Nexus

SNPshotrs587777761
SNPdbers587777761
MSV3drs587777761
GWAS Ctlgrs587777761
Max Magnitude0
ClinVar
Risk rs587777761(;)
Alt rs587777761(;)
Reference rs587777761(A;A)
Significance Pathogenic
Disease Familial visceral amyloidosis
Variation info
Gene FGA
CLNDBN Familial visceral amyloidosis, Ostertag type
Reversed 0
HGVS NC_000004.11:g.155506959delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000017870.28,