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rs398123422

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123422(A;A)
Make rs398123422(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77698573
GeneATRX
is asnp
is mentioned by
dbSNPrs398123422
ebirs398123422
HLIrs398123422
Exacrs398123422
Varsomers398123422
Maprs398123422
PheGenIrs398123422
hapmaprs398123422
1000 genomesrs398123422
hgdprs398123422
ensemblrs398123422
gopubmedrs398123422
geneviewrs398123422
scholarrs398123422
googlers398123422
pharmgkbrs398123422
gwascentralrs398123422
openSNPrs398123422
23andMers398123422
23andMe allrs398123422
SNP Nexus

SNPshotrs398123422
SNPdbers398123422
MSV3drs398123422
GWAS Ctlgrs398123422
Max Magnitude0
ClinVar
Risk rs398123422(A;A)
Alt rs398123422(A;A)
Reference rs398123422(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ATRX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.76954061C>T
CLNSRC ClinVar
CLNACC RCV000078957.4,