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rs780327716

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs780327716(-;-)
Make rs780327716(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51964959
GeneATP7B
is asnp
is mentioned by
dbSNPrs780327716
ebirs780327716
HLIrs780327716
Exacrs780327716
Varsomers780327716
Maprs780327716
PheGenIrs780327716
hapmaprs780327716
1000 genomesrs780327716
hgdprs780327716
ensemblrs780327716
gopubmedrs780327716
geneviewrs780327716
scholarrs780327716
googlers780327716
pharmgkbrs780327716
gwascentralrs780327716
openSNPrs780327716
23andMers780327716
23andMe allrs780327716
SNP Nexus

SNPshotrs780327716
SNPdbers780327716
MSV3drs780327716
GWAS Ctlgrs780327716
Max Magnitude0
ClinVar
Risk rs780327716(;)
Alt rs780327716(;)
Reference rs780327716(A;A)
Significance Probable-Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 0
HGVS NC_000013.10:g.52539095delA
CLNSRC
CLNACC RCV000169497.1,