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rs387906823

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906823(A;C)
Make rs387906823(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position38925249
GeneOSMR
is asnp
is mentioned by
dbSNPrs387906823
ebirs387906823
HLIrs387906823
Exacrs387906823
Varsomers387906823
Maprs387906823
PheGenIrs387906823
hapmaprs387906823
1000 genomesrs387906823
hgdprs387906823
ensemblrs387906823
gopubmedrs387906823
geneviewrs387906823
scholarrs387906823
googlers387906823
pharmgkbrs387906823
gwascentralrs387906823
openSNPrs387906823
23andMers387906823
23andMe allrs387906823
SNP Nexus

SNPshotrs387906823
SNPdbers387906823
MSV3drs387906823
GWAS Ctlgrs387906823
Max Magnitude0
ClinVar
Risk rs387906823(C,G;C,G)
Alt rs387906823(C,G;C,G)
Reference rs387906823(A;A)
Significance Pathogenic
Disease Primary localized cutaneous amyloidosis 1
Variation info
Gene OSMR
CLNDBN Primary localized cutaneous amyloidosis 1
Reversed 0
HGVS NC_000005.9:g.38925351A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023145.3,