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rs1057517971

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517971(-;-)
Make rs1057517971(-;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position69616553
GeneEDA
is asnp
is mentioned by
dbSNPrs1057517971
dbSNP (old)rs1057517971
ClinGenrs1057517971
ebirs1057517971
HLIrs1057517971
Exacrs1057517971
Gnomadrs1057517971
Varsomers1057517971
Maprs1057517971
PheGenIrs1057517971
Biobankrs1057517971
1000 genomesrs1057517971
hgdprs1057517971
ensemblrs1057517971
gopubmedrs1057517971
geneviewrs1057517971
scholarrs1057517971
googlers1057517971
pharmgkbrs1057517971
gwascentralrs1057517971
openSNPrs1057517971
23andMers1057517971
23andMe allrs1057517971
SNPshotrs1057517971
SNPdbers1057517971
MSV3drs1057517971
GWAS Ctlgrs1057517971
Max Magnitude0
ClinVar
Risk rs1057517971(-;-)
Alt rs1057517971(-;-)
Reference Rs1057517971(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene EDA
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.68836397delG
CLNSRC
CLNACC RCV000413757.1,