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rs756029120

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs756029120(C;T)
Make rs756029120(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51941120
GeneATP7B
is asnp
is mentioned by
dbSNPrs756029120
ebirs756029120
HLIrs756029120
Exacrs756029120
Varsomers756029120
Maprs756029120
PheGenIrs756029120
hapmaprs756029120
1000 genomesrs756029120
hgdprs756029120
ensemblrs756029120
gopubmedrs756029120
geneviewrs756029120
scholarrs756029120
googlers756029120
pharmgkbrs756029120
gwascentralrs756029120
openSNPrs756029120
23andMers756029120
23andMe allrs756029120
SNP Nexus

SNPshotrs756029120
SNPdbers756029120
MSV3drs756029120
GWAS Ctlgrs756029120
Max Magnitude0
ClinVar
Risk rs756029120(T;T)
Alt rs756029120(T;T)
Reference rs756029120(C;C)
Significance Probable-Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 0
HGVS NC_000013.10:g.52515256C>T
CLNSRC
CLNACC RCV000169445.1,