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rs72552285

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72552285(C;C)
Make rs72552285(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51961859
GeneATP7B
is asnp
is mentioned by
dbSNPrs72552285
ebirs72552285
HLIrs72552285
Exacrs72552285
Varsomers72552285
Maprs72552285
PheGenIrs72552285
hapmaprs72552285
1000 genomesrs72552285
hgdprs72552285
ensemblrs72552285
gopubmedrs72552285
geneviewrs72552285
scholarrs72552285
googlers72552285
pharmgkbrs72552285
gwascentralrs72552285
openSNPrs72552285
23andMers72552285
23andMe allrs72552285
SNP Nexus

SNPshotrs72552285
SNPdbers72552285
MSV3drs72552285
GWAS Ctlgrs72552285
Max Magnitude0
ClinVar
Risk rs72552285(A,C;A,C)
Alt rs72552285(A,C;A,C)
Reference rs72552285(G;G)
Significance Probable-Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 1
HGVS NC_000013.10:g.52535995C>G
CLNSRC
CLNACC RCV000169521.1,