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

rs1057517731

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517731(G;T)
Make rs1057517731(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position70033431
GeneEDA
is asnp
is mentioned by
dbSNPrs1057517731
dbSNP (old)rs1057517731
ClinGenrs1057517731
ebirs1057517731
HLIrs1057517731
Exacrs1057517731
Gnomadrs1057517731
Varsomers1057517731
Maprs1057517731
PheGenIrs1057517731
Biobankrs1057517731
1000 genomesrs1057517731
hgdprs1057517731
ensemblrs1057517731
gopubmedrs1057517731
geneviewrs1057517731
scholarrs1057517731
googlers1057517731
pharmgkbrs1057517731
gwascentralrs1057517731
openSNPrs1057517731
23andMers1057517731
23andMe allrs1057517731
SNPshotrs1057517731
SNPdbers1057517731
MSV3drs1057517731
GWAS Ctlgrs1057517731
Max Magnitude0
ClinVar
Risk rs1057517731(T;T)
Alt rs1057517731(T;T)
Reference Rs1057517731(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EDA
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.69253281G>T
CLNSRC
CLNACC RCV000413141.1,