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rs193922108

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922108(G;T)
Make rs193922108(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position51937679
GeneATP7B
is asnp
is mentioned by
dbSNPrs193922108
ebirs193922108
HLIrs193922108
Exacrs193922108
Varsomers193922108
Maprs193922108
PheGenIrs193922108
hapmaprs193922108
1000 genomesrs193922108
hgdprs193922108
ensemblrs193922108
gopubmedrs193922108
geneviewrs193922108
scholarrs193922108
googlers193922108
pharmgkbrs193922108
gwascentralrs193922108
openSNPrs193922108
23andMers193922108
23andMe allrs193922108
SNP Nexus

SNPshotrs193922108
SNPdbers193922108
MSV3drs193922108
GWAS Ctlgrs193922108
Max Magnitude0
ClinVar
Risk rs193922108(T;T)
Alt rs193922108(T;T)
Reference rs193922108(G;G)
Significance Probable-Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 1
HGVS NC_000013.10:g.52511815C>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029375.1,