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rs1057518225

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518225(C;C)
Make rs1057518225(C;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position77520841
GeneATRX
is asnp
is mentioned by
dbSNPrs1057518225
dbSNP (old)rs1057518225
ClinGenrs1057518225
ebirs1057518225
HLIrs1057518225
Exacrs1057518225
Gnomadrs1057518225
Varsomers1057518225
LitVarrs1057518225
Maprs1057518225
PheGenIrs1057518225
Biobankrs1057518225
1000 genomesrs1057518225
hgdprs1057518225
ensemblrs1057518225
gopubmedrs1057518225
geneviewrs1057518225
scholarrs1057518225
googlers1057518225
pharmgkbrs1057518225
gwascentralrs1057518225
openSNPrs1057518225
23andMers1057518225
23andMe allrs1057518225
SNPshotrs1057518225
SNPdbers1057518225
MSV3drs1057518225
GWAS Ctlgrs1057518225
Max Magnitude0
ClinVar
Risk rs1057518225(C;C)
Alt rs1057518225(C;C)
Reference Rs1057518225(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATRX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.76776319C>G
CLNSRC
CLNACC RCV000414709.1,