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rs1057524153

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524153(C;G)
Make rs1057524153(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position77684527
GeneATRX
is asnp
is mentioned by
dbSNPrs1057524153
dbSNP (old)rs1057524153
ClinGenrs1057524153
ebirs1057524153
HLIrs1057524153
Exacrs1057524153
Gnomadrs1057524153
Varsomers1057524153
Maprs1057524153
PheGenIrs1057524153
Biobankrs1057524153
1000 genomesrs1057524153
hgdprs1057524153
ensemblrs1057524153
gopubmedrs1057524153
geneviewrs1057524153
scholarrs1057524153
googlers1057524153
pharmgkbrs1057524153
gwascentralrs1057524153
openSNPrs1057524153
23andMers1057524153
23andMe allrs1057524153
SNPshotrs1057524153
SNPdbers1057524153
MSV3drs1057524153
GWAS Ctlgrs1057524153
Max Magnitude0
ClinVar
Risk rs1057524153(G;G)
Alt rs1057524153(G;G)
Reference Rs1057524153(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATRX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.76940019G>C
CLNSRC
CLNACC RCV000419781.1,