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rs1057518211

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518211(A;C)
Make rs1057518211(C;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position70035365
GeneEDA
is asnp
is mentioned by
dbSNPrs1057518211
dbSNP (old)rs1057518211
ClinGenrs1057518211
ebirs1057518211
HLIrs1057518211
Exacrs1057518211
Gnomadrs1057518211
Varsomers1057518211
Maprs1057518211
PheGenIrs1057518211
Biobankrs1057518211
1000 genomesrs1057518211
hgdprs1057518211
ensemblrs1057518211
gopubmedrs1057518211
geneviewrs1057518211
scholarrs1057518211
googlers1057518211
pharmgkbrs1057518211
gwascentralrs1057518211
openSNPrs1057518211
23andMers1057518211
23andMe allrs1057518211
SNPshotrs1057518211
SNPdbers1057518211
MSV3drs1057518211
GWAS Ctlgrs1057518211
Max Magnitude0
ClinVar
Risk rs1057518211(C;C)
Alt rs1057518211(C;C)
Reference Rs1057518211(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EDA
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.69255215A>C
CLNSRC
CLNACC RCV000414008.1,