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rs387906822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906822(C;T)
Make rs387906822(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position38925240
GeneOSMR
is asnp
is mentioned by
dbSNPrs387906822
ebirs387906822
HLIrs387906822
Exacrs387906822
Varsomers387906822
Maprs387906822
PheGenIrs387906822
hapmaprs387906822
1000 genomesrs387906822
hgdprs387906822
ensemblrs387906822
gopubmedrs387906822
geneviewrs387906822
scholarrs387906822
googlers387906822
pharmgkbrs387906822
gwascentralrs387906822
openSNPrs387906822
23andMers387906822
23andMe allrs387906822
SNP Nexus

SNPshotrs387906822
SNPdbers387906822
MSV3drs387906822
GWAS Ctlgrs387906822
Max Magnitude0
ClinVar
Risk rs387906822(T;T)
Alt rs387906822(T;T)
Reference rs387906822(C;C)
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.38925342C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023144.2,