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rs398123420

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123420(A;G)
Make rs398123420(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77698631
GeneATRX
is asnp
is mentioned by
dbSNPrs398123420
ebirs398123420
HLIrs398123420
Exacrs398123420
Varsomers398123420
Maprs398123420
PheGenIrs398123420
hapmaprs398123420
1000 genomesrs398123420
hgdprs398123420
ensemblrs398123420
gopubmedrs398123420
geneviewrs398123420
scholarrs398123420
googlers398123420
pharmgkbrs398123420
gwascentralrs398123420
openSNPrs398123420
23andMers398123420
23andMe allrs398123420
SNP Nexus

SNPshotrs398123420
SNPdbers398123420
MSV3drs398123420
GWAS Ctlgrs398123420
Max Magnitude0
ClinVar
Risk rs398123420(G;G)
Alt rs398123420(G;G)
Reference rs398123420(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ATRX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.76954119T>C
CLNSRC ClinVar
CLNACC RCV000078954.4,