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rs1057517707

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517707(C;T)
Make rs1057517707(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position77557618
GeneATRX
is asnp
is mentioned by
dbSNPrs1057517707
dbSNP (old)rs1057517707
ClinGenrs1057517707
ebirs1057517707
HLIrs1057517707
Exacrs1057517707
Gnomadrs1057517707
Varsomers1057517707
Maprs1057517707
PheGenIrs1057517707
Biobankrs1057517707
1000 genomesrs1057517707
hgdprs1057517707
ensemblrs1057517707
gopubmedrs1057517707
geneviewrs1057517707
scholarrs1057517707
googlers1057517707
pharmgkbrs1057517707
gwascentralrs1057517707
openSNPrs1057517707
23andMers1057517707
23andMe allrs1057517707
SNPshotrs1057517707
SNPdbers1057517707
MSV3drs1057517707
GWAS Ctlgrs1057517707
Max Magnitude0
ClinVar
Risk rs1057517707(T;T)
Alt rs1057517707(T;T)
Reference Rs1057517707(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATRX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.76813089G>A
CLNSRC
CLNACC RCV000414248.1,