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rs1057517997

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517997(A;T)
Make rs1057517997(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position77652162
GeneATRX
is asnp
is mentioned by
dbSNPrs1057517997
dbSNP (old)rs1057517997
ClinGenrs1057517997
ebirs1057517997
HLIrs1057517997
Exacrs1057517997
Gnomadrs1057517997
Varsomers1057517997
Maprs1057517997
PheGenIrs1057517997
Biobankrs1057517997
1000 genomesrs1057517997
hgdprs1057517997
ensemblrs1057517997
gopubmedrs1057517997
geneviewrs1057517997
scholarrs1057517997
googlers1057517997
pharmgkbrs1057517997
gwascentralrs1057517997
openSNPrs1057517997
23andMers1057517997
23andMe allrs1057517997
SNPshotrs1057517997
SNPdbers1057517997
MSV3drs1057517997
GWAS Ctlgrs1057517997
Max Magnitude0
ClinVar
Risk rs1057517997(T;T)
Alt rs1057517997(T;T)
Reference Rs1057517997(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATRX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.76907652T>A
CLNSRC
CLNACC RCV000413791.1,