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rs1057517948

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517948(A;A)
Make rs1057517948(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position77574322
GeneATRX
is asnp
is mentioned by
dbSNPrs1057517948
dbSNP (classic)rs1057517948
ClinGenrs1057517948
ebirs1057517948
HLIrs1057517948
Exacrs1057517948
Gnomadrs1057517948
Varsomers1057517948
LitVarrs1057517948
Maprs1057517948
PheGenIrs1057517948
Biobankrs1057517948
1000 genomesrs1057517948
hgdprs1057517948
ensemblrs1057517948
geneviewrs1057517948
scholarrs1057517948
googlers1057517948
pharmgkbrs1057517948
gwascentralrs1057517948
openSNPrs1057517948
23andMers1057517948
23andMe allrs1057517948
SNPshotrs1057517948
SNPdbers1057517948
MSV3drs1057517948
GWAS Ctlgrs1057517948
Max Magnitude0
ClinVar
Risk rs1057517948(A;A)
Alt rs1057517948(A;A)
Reference Rs1057517948(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATRX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.76829787C>T
CLNSRC
CLNACC RCV000413472.1,