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rs78506343

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs78506343(G;T)
Make rs78506343(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154585711
GeneFGA
is asnp
is mentioned by
dbSNPrs78506343
ebirs78506343
HLIrs78506343
Exacrs78506343
Varsomers78506343
Maprs78506343
PheGenIrs78506343
hapmaprs78506343
1000 genomesrs78506343
hgdprs78506343
ensemblrs78506343
gopubmedrs78506343
geneviewrs78506343
scholarrs78506343
googlers78506343
pharmgkbrs78506343
gwascentralrs78506343
openSNPrs78506343
23andMers78506343
23andMe allrs78506343
SNP Nexus

SNPshotrs78506343
SNPdbers78506343
MSV3drs78506343
GWAS Ctlgrs78506343
Max Magnitude0
OMIM134820
Desc
Variant0012
Relatedalso
ClinVar
Risk rs78506343(A,T;A,T)
Alt rs78506343(A,T;A,T)
Reference rs78506343(G;G)
Significance Pathogenic
Disease Familial visceral amyloidosis
Variation info
Gene FGA
CLNDBN Familial visceral amyloidosis, Ostertag type
Reversed 1
HGVS NC_000004.11:g.155506863C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017869.28,