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rs398123135

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123135(G;T)
Make rs398123135(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position78042584
GeneATP7A
is asnp
is mentioned by
dbSNPrs398123135
ebirs398123135
HLIrs398123135
Exacrs398123135
Varsomers398123135
Maprs398123135
PheGenIrs398123135
hapmaprs398123135
1000 genomesrs398123135
hgdprs398123135
ensemblrs398123135
gopubmedrs398123135
geneviewrs398123135
scholarrs398123135
googlers398123135
pharmgkbrs398123135
gwascentralrs398123135
openSNPrs398123135
23andMers398123135
23andMe allrs398123135
SNP Nexus

SNPshotrs398123135
SNPdbers398123135
MSV3drs398123135
GWAS Ctlgrs398123135
Max Magnitude0
ClinVar
Risk rs398123135(T;T)
Alt rs398123135(T;T)
Reference rs398123135(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ATP7A
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.77298082G>T
CLNSRC ClinVar
CLNACC RCV000078035.4,