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rs398123425

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123425(A;G)
Make rs398123425(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77688876
GeneATRX
is asnp
is mentioned by
dbSNPrs398123425
dbSNP (old)rs398123425
ClinGenrs398123425
ebirs398123425
HLIrs398123425
Exacrs398123425
Gnomadrs398123425
Varsomers398123425
Maprs398123425
PheGenIrs398123425
Biobankrs398123425
1000 genomesrs398123425
hgdprs398123425
ensemblrs398123425
gopubmedrs398123425
geneviewrs398123425
scholarrs398123425
googlers398123425
pharmgkbrs398123425
gwascentralrs398123425
openSNPrs398123425
23andMers398123425
23andMe allrs398123425
SNP Nexus

SNPshotrs398123425
SNPdbers398123425
MSV3drs398123425
GWAS Ctlgrs398123425
Max Magnitude0
ClinVar
Risk rs398123425(G;G)
Alt rs398123425(G;G)
Reference Rs398123425(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ATRX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.76944369T>C
CLNSRC HGMD
CLNACC RCV000078965.5,