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rs587777762

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777762(-;-)
Make rs587777762(-;C)
ReferenceGRCh38 38.1/142
Chromosome4
Position154585800
GeneFGA
is asnp
is mentioned by
dbSNPrs587777762
ebirs587777762
HLIrs587777762
Exacrs587777762
Varsomers587777762
Maprs587777762
PheGenIrs587777762
hapmaprs587777762
1000 genomesrs587777762
hgdprs587777762
ensemblrs587777762
gopubmedrs587777762
geneviewrs587777762
scholarrs587777762
googlers587777762
pharmgkbrs587777762
gwascentralrs587777762
openSNPrs587777762
23andMers587777762
23andMe allrs587777762
SNP Nexus

SNPshotrs587777762
SNPdbers587777762
MSV3drs587777762
GWAS Ctlgrs587777762
Max Magnitude0
ClinVar
Risk rs587777762(;)
Alt rs587777762(;)
Reference rs587777762(C;C)
Significance Pathogenic
Disease Familial visceral amyloidosis
Variation info
Gene FGA
CLNDBN Familial visceral amyloidosis, Ostertag type
Reversed 0
HGVS NC_000004.11:g.155506952delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000017875.24,