Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057524693

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524693(A;A)
Make rs1057524693(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position119575374
GeneUBE2A
is asnp
is mentioned by
dbSNPrs1057524693
dbSNP (old)rs1057524693
ClinGenrs1057524693
ebirs1057524693
HLIrs1057524693
Exacrs1057524693
Gnomadrs1057524693
Varsomers1057524693
Maprs1057524693
PheGenIrs1057524693
Biobankrs1057524693
1000 genomesrs1057524693
hgdprs1057524693
ensemblrs1057524693
gopubmedrs1057524693
geneviewrs1057524693
scholarrs1057524693
googlers1057524693
pharmgkbrs1057524693
gwascentralrs1057524693
openSNPrs1057524693
23andMers1057524693
23andMe allrs1057524693
SNPshotrs1057524693
SNPdbers1057524693
MSV3drs1057524693
GWAS Ctlgrs1057524693
Max Magnitude0
ClinVar
Risk rs1057524693(A;A)
Alt rs1057524693(A;A)
Reference Rs1057524693(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene UBE2A
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.118709337G>A
CLNSRC
CLNACC RCV000432035.1,