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rs398123133

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123133(-;-)
Make rs398123133(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77989827
GeneATP7A
is asnp
is mentioned by
dbSNPrs398123133
ebirs398123133
HLIrs398123133
Exacrs398123133
Varsomers398123133
Maprs398123133
PheGenIrs398123133
hapmaprs398123133
1000 genomesrs398123133
hgdprs398123133
ensemblrs398123133
gopubmedrs398123133
geneviewrs398123133
scholarrs398123133
googlers398123133
pharmgkbrs398123133
gwascentralrs398123133
openSNPrs398123133
23andMers398123133
23andMe allrs398123133
SNP Nexus

SNPshotrs398123133
SNPdbers398123133
MSV3drs398123133
GWAS Ctlgrs398123133
Max Magnitude0
ClinVar
Risk rs398123133(;)
Alt rs398123133(;)
Reference rs398123133(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ATP7A
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.77245323delA
CLNSRC ClinVar
CLNACC RCV000078031.4,