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rs397516681

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516681(A;G)
Make rs397516681(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position70033506
GeneEDA
is asnp
is mentioned by
dbSNPrs397516681
ebirs397516681
HLIrs397516681
Exacrs397516681
Varsomers397516681
Maprs397516681
PheGenIrs397516681
hapmaprs397516681
1000 genomesrs397516681
hgdprs397516681
ensemblrs397516681
gopubmedrs397516681
geneviewrs397516681
scholarrs397516681
googlers397516681
pharmgkbrs397516681
gwascentralrs397516681
openSNPrs397516681
23andMers397516681
23andMe allrs397516681
SNP Nexus

SNPshotrs397516681
SNPdbers397516681
MSV3drs397516681
GWAS Ctlgrs397516681
Max Magnitude0
ClinVar
Risk rs397516681(G;G)
Alt rs397516681(G;G)
Reference rs397516681(A;A)
Significance Probable-Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.69253356A>G
CLNSRC ClinVar
CLNACC RCV000037193.2,