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rs797044563

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044563(A;A)
Make rs797044563(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position77683154
GeneATRX
is asnp
is mentioned by
dbSNPrs797044563
ebirs797044563
HLIrs797044563
Exacrs797044563
Varsomers797044563
Maprs797044563
PheGenIrs797044563
hapmaprs797044563
1000 genomesrs797044563
hgdprs797044563
ensemblrs797044563
gopubmedrs797044563
geneviewrs797044563
scholarrs797044563
googlers797044563
pharmgkbrs797044563
gwascentralrs797044563
openSNPrs797044563
23andMers797044563
23andMe allrs797044563
SNP Nexus

SNPshotrs797044563
SNPdbers797044563
MSV3drs797044563
GWAS Ctlgrs797044563
Max Magnitude0
ClinVar
Risk rs797044563(A;A)
Alt rs797044563(A;A)
Reference rs797044563(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATRX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.76938646C>T
CLNSRC
CLNACC RCV000171440.1,