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rs398122820

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122820(A;A)
Make rs398122820(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position44715641
GeneB2M
is asnp
is mentioned by
dbSNPrs398122820
ebirs398122820
HLIrs398122820
Exacrs398122820
Varsomers398122820
Maprs398122820
PheGenIrs398122820
hapmaprs398122820
1000 genomesrs398122820
hgdprs398122820
ensemblrs398122820
gopubmedrs398122820
geneviewrs398122820
scholarrs398122820
googlers398122820
pharmgkbrs398122820
gwascentralrs398122820
openSNPrs398122820
23andMers398122820
23andMe allrs398122820
SNP Nexus

SNPshotrs398122820
SNPdbers398122820
MSV3drs398122820
GWAS Ctlgrs398122820
Max Magnitude0
ClinVar
Risk rs398122820(A;A)
Alt rs398122820(A;A)
Reference rs398122820(G;G)
Significance Pathogenic
Disease Familial visceral amyloidosis
Variation info
Gene B2M
CLNDBN Familial visceral amyloidosis, Ostertag type
Reversed 0
HGVS NC_000015.9:g.45007839G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000024598.27,