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rs371840514

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs371840514(A;A)
Make rs371840514(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51946291
GeneATP7B
is asnp
is mentioned by
dbSNPrs371840514
ebirs371840514
HLIrs371840514
Exacrs371840514
Varsomers371840514
Maprs371840514
PheGenIrs371840514
hapmaprs371840514
1000 genomesrs371840514
hgdprs371840514
ensemblrs371840514
gopubmedrs371840514
geneviewrs371840514
scholarrs371840514
googlers371840514
pharmgkbrs371840514
gwascentralrs371840514
openSNPrs371840514
23andMers371840514
23andMe allrs371840514
SNP Nexus

SNPshotrs371840514
SNPdbers371840514
MSV3drs371840514
GWAS Ctlgrs371840514
Max Magnitude0
ClinVar
Risk rs371840514(A;A)
Alt rs371840514(A;A)
Reference rs371840514(G;G)
Significance Probable-Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 0
HGVS NC_000013.10:g.52520427G>A
CLNSRC
CLNACC RCV000169019.1,