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rs1060499658

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499658(A;A)
Make rs1060499658(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position77589929
GeneATRX
is asnp
is mentioned by
dbSNPrs1060499658
dbSNP (old)rs1060499658
ClinGenrs1060499658
ebirs1060499658
HLIrs1060499658
Exacrs1060499658
Gnomadrs1060499658
Varsomers1060499658
Maprs1060499658
PheGenIrs1060499658
Biobankrs1060499658
1000 genomesrs1060499658
hgdprs1060499658
ensemblrs1060499658
gopubmedrs1060499658
geneviewrs1060499658
scholarrs1060499658
googlers1060499658
pharmgkbrs1060499658
gwascentralrs1060499658
openSNPrs1060499658
23andMers1060499658
23andMe allrs1060499658
SNPshotrs1060499658
SNPdbers1060499658
MSV3drs1060499658
GWAS Ctlgrs1060499658
Max Magnitude0
ClinVar
Risk rs1060499658(A;A)
Alt rs1060499658(A;A)
Reference Rs1060499658(G;G)
Significance Pathogenic
Disease ATR-X syndrome
Variation info
Gene ATRX
CLNDBN ATR-X syndrome
Reversed 1
HGVS NC_000023.10:g.76845399C>T
CLNSRC
CLNACC RCV000449558.1,