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rs1057517882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517882(C;C)
Make rs1057517882(C;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position70030496
GeneEDA
is asnp
is mentioned by
dbSNPrs1057517882
dbSNP (old)rs1057517882
ClinGenrs1057517882
ebirs1057517882
HLIrs1057517882
Exacrs1057517882
Gnomadrs1057517882
Varsomers1057517882
Maprs1057517882
PheGenIrs1057517882
Biobankrs1057517882
1000 genomesrs1057517882
hgdprs1057517882
ensemblrs1057517882
gopubmedrs1057517882
geneviewrs1057517882
scholarrs1057517882
googlers1057517882
pharmgkbrs1057517882
gwascentralrs1057517882
openSNPrs1057517882
23andMers1057517882
23andMe allrs1057517882
SNPshotrs1057517882
SNPdbers1057517882
MSV3drs1057517882
GWAS Ctlgrs1057517882
Max Magnitude0
ClinVar
Risk rs1057517882(C;C)
Alt rs1057517882(C;C)
Reference Rs1057517882(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EDA
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.69250346G>C
CLNSRC
CLNACC RCV000413515.1,