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rs786204578

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204578(C;T)
Make rs786204578(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position51935666
GeneATP7B
is asnp
is mentioned by
dbSNPrs786204578
ebirs786204578
HLIrs786204578
Exacrs786204578
Varsomers786204578
Maprs786204578
PheGenIrs786204578
hapmaprs786204578
1000 genomesrs786204578
hgdprs786204578
ensemblrs786204578
gopubmedrs786204578
geneviewrs786204578
scholarrs786204578
googlers786204578
pharmgkbrs786204578
gwascentralrs786204578
openSNPrs786204578
23andMers786204578
23andMe allrs786204578
SNP Nexus

SNPshotrs786204578
SNPdbers786204578
MSV3drs786204578
GWAS Ctlgrs786204578
Max Magnitude0
ClinVar
Risk rs786204578(T;T)
Alt rs786204578(T;T)
Reference rs786204578(C;C)
Significance Probable-Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 1
HGVS NC_000013.10:g.52509802G>A
CLNSRC
CLNACC RCV000169321.1,