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rs755709270

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs755709270(-;-)
Make rs755709270(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51950315
GeneATP7B
is asnp
is mentioned by
dbSNPrs755709270
ebirs755709270
HLIrs755709270
Exacrs755709270
Varsomers755709270
Maprs755709270
PheGenIrs755709270
hapmaprs755709270
1000 genomesrs755709270
hgdprs755709270
ensemblrs755709270
gopubmedrs755709270
geneviewrs755709270
scholarrs755709270
googlers755709270
pharmgkbrs755709270
gwascentralrs755709270
openSNPrs755709270
23andMers755709270
23andMe allrs755709270
SNP Nexus

SNPshotrs755709270
SNPdbers755709270
MSV3drs755709270
GWAS Ctlgrs755709270
Max Magnitude0
ClinVar
Risk rs755709270(;)
Alt rs755709270(;)
Reference rs755709270(T;T)
Significance Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 0
HGVS NC_000013.10:g.52524451delT
CLNSRC
CLNACC RCV000169237.2,