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rs768671894

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs768671894(A;A)
Make rs768671894(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51950328
GeneATP7B
is asnp
is mentioned by
dbSNPrs768671894
ebirs768671894
HLIrs768671894
Exacrs768671894
Varsomers768671894
Maprs768671894
PheGenIrs768671894
hapmaprs768671894
1000 genomesrs768671894
hgdprs768671894
ensemblrs768671894
gopubmedrs768671894
geneviewrs768671894
scholarrs768671894
googlers768671894
pharmgkbrs768671894
gwascentralrs768671894
openSNPrs768671894
23andMers768671894
23andMe allrs768671894
SNP Nexus

SNPshotrs768671894
SNPdbers768671894
MSV3drs768671894
GWAS Ctlgrs768671894
Max Magnitude0
ClinVar
Risk rs768671894(A;A)
Alt rs768671894(A;A)
Reference rs768671894(G;G)
Significance Probable-Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 0
HGVS NC_000013.10:g.52524464G>A
CLNSRC
CLNACC RCV000169233.1,