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rs753962912

From SNPedia

Orientationplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs753962912(-;-)
Make rs753962912(-;TA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51964995
GeneATP7B
is asnp
is mentioned by
dbSNPrs753962912
ebirs753962912
HLIrs753962912
Exacrs753962912
Varsomers753962912
Maprs753962912
PheGenIrs753962912
hapmaprs753962912
1000 genomesrs753962912
hgdprs753962912
ensemblrs753962912
gopubmedrs753962912
geneviewrs753962912
scholarrs753962912
googlers753962912
pharmgkbrs753962912
gwascentralrs753962912
openSNPrs753962912
23andMers753962912
23andMe allrs753962912
SNP Nexus

SNPshotrs753962912
SNPdbers753962912
MSV3drs753962912
GWAS Ctlgrs753962912
Max Magnitude0
ClinVar
Risk rs753962912(;)
Alt rs753962912(;)
Reference rs753962912(TA;TA)
Significance Probable-Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 0
HGVS NC_000013.10:g.52539131_52539132delTA
CLNSRC
CLNACC RCV000169524.1,