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rs28942075

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in clinvar
Make rs28942075(A;A)
Make rs28942075(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position51958373
GeneATP7B
is asnp
is mentioned by
dbSNPrs28942075
ebirs28942075
HLIrs28942075
Exacrs28942075
Varsomers28942075
Maprs28942075
PheGenIrs28942075
hapmaprs28942075
1000 genomesrs28942075
hgdprs28942075
ensemblrs28942075
gopubmedrs28942075
geneviewrs28942075
scholarrs28942075
googlers28942075
pharmgkbrs28942075
gwascentralrs28942075
openSNPrs28942075
23andMers28942075
23andMe allrs28942075
SNP Nexus

SNPshotrs28942075
SNPdbers28942075
MSV3drs28942075
GWAS Ctlgrs28942075
Max Magnitude0
OMIM606882
DescWILSON DISEASE
Variant0012
Relatedalso
Neighborrs28942074
Distance40


ClinVar
Risk rs28942075(A,C;A,C)
Alt rs28942075(A,C;A,C)
Reference rs28942075(G;G)
Significance Other
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 1
HGVS NC_000013.10:g.52532509C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004059.4,