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rs387906535

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906535(C;C)
Make rs387906535(C;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position69350170
GeneLYZ
is asnp
is mentioned by
dbSNPrs387906535
ebirs387906535
HLIrs387906535
Exacrs387906535
Varsomers387906535
Maprs387906535
PheGenIrs387906535
hapmaprs387906535
1000 genomesrs387906535
hgdprs387906535
ensemblrs387906535
gopubmedrs387906535
geneviewrs387906535
scholarrs387906535
googlers387906535
pharmgkbrs387906535
gwascentralrs387906535
openSNPrs387906535
23andMers387906535
23andMe allrs387906535
SNP Nexus

SNPshotrs387906535
SNPdbers387906535
MSV3drs387906535
GWAS Ctlgrs387906535
Max Magnitude0
ClinVar
Risk rs387906535(C;C)
Alt rs387906535(C;C)
Reference rs387906535(G;G)
Significance Pathogenic
Disease Familial visceral amyloidosis
Variation info
Gene LYZ
CLNDBN Familial visceral amyloidosis, Ostertag type
Reversed 0
HGVS NC_000012.11:g.69743950G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000015451.25,