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rs1057521131

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521131(C;C)
Make rs1057521131(C;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position69957124
GeneEDA
is asnp
is mentioned by
dbSNPrs1057521131
dbSNP (old)rs1057521131
ClinGenrs1057521131
ebirs1057521131
HLIrs1057521131
Exacrs1057521131
Gnomadrs1057521131
Varsomers1057521131
Maprs1057521131
PheGenIrs1057521131
Biobankrs1057521131
1000 genomesrs1057521131
hgdprs1057521131
ensemblrs1057521131
gopubmedrs1057521131
geneviewrs1057521131
scholarrs1057521131
googlers1057521131
pharmgkbrs1057521131
gwascentralrs1057521131
openSNPrs1057521131
23andMers1057521131
23andMe allrs1057521131
SNPshotrs1057521131
SNPdbers1057521131
MSV3drs1057521131
GWAS Ctlgrs1057521131
Max Magnitude0
ClinVar
Risk rs1057521131(C;C)
Alt rs1057521131(C;C)
Reference Rs1057521131(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EDA
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.69176974G>C
CLNSRC
CLNACC RCV000432953.1,