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rs759749626

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs759749626(A;T)
Make rs759749626(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51973933
GeneATP7B
is asnp
is mentioned by
dbSNPrs759749626
ebirs759749626
HLIrs759749626
Exacrs759749626
Varsomers759749626
Maprs759749626
PheGenIrs759749626
hapmaprs759749626
1000 genomesrs759749626
hgdprs759749626
ensemblrs759749626
gopubmedrs759749626
geneviewrs759749626
scholarrs759749626
googlers759749626
pharmgkbrs759749626
gwascentralrs759749626
openSNPrs759749626
23andMers759749626
23andMe allrs759749626
SNP Nexus

SNPshotrs759749626
SNPdbers759749626
MSV3drs759749626
GWAS Ctlgrs759749626
Max Magnitude0
ClinVar
Risk rs759749626(T;T)
Alt rs759749626(T;T)
Reference rs759749626(A;A)
Significance Probable-Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 0
HGVS NC_000013.10:g.52548069A>T
CLNSRC
CLNACC RCV000169532.1,