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rs1057520742

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520742(C;T)
Make rs1057520742(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position70027947
GeneEDA
is asnp
is mentioned by
dbSNPrs1057520742
dbSNP (old)rs1057520742
ClinGenrs1057520742
ebirs1057520742
HLIrs1057520742
Exacrs1057520742
Gnomadrs1057520742
Varsomers1057520742
Maprs1057520742
PheGenIrs1057520742
Biobankrs1057520742
1000 genomesrs1057520742
hgdprs1057520742
ensemblrs1057520742
gopubmedrs1057520742
geneviewrs1057520742
scholarrs1057520742
googlers1057520742
pharmgkbrs1057520742
gwascentralrs1057520742
openSNPrs1057520742
23andMers1057520742
23andMe allrs1057520742
SNPshotrs1057520742
SNPdbers1057520742
MSV3drs1057520742
GWAS Ctlgrs1057520742
Max Magnitude0
ClinVar
Risk rs1057520742(T;T)
Alt rs1057520742(T;T)
Reference Rs1057520742(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene EDA
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.69247797C>T
CLNSRC
CLNACC RCV000439320.1,