Have questions? Visit https://www.reddit.com/r/SNPedia

rs397516657

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516657(A;A)
Make rs397516657(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position69616472
GeneEDA
is asnp
is mentioned by
dbSNPrs397516657
ebirs397516657
HLIrs397516657
Exacrs397516657
Varsomers397516657
Maprs397516657
PheGenIrs397516657
hapmaprs397516657
1000 genomesrs397516657
hgdprs397516657
ensemblrs397516657
gopubmedrs397516657
geneviewrs397516657
scholarrs397516657
googlers397516657
pharmgkbrs397516657
gwascentralrs397516657
openSNPrs397516657
23andMers397516657
23andMe allrs397516657
SNP Nexus

SNPshotrs397516657
SNPdbers397516657
MSV3drs397516657
GWAS Ctlgrs397516657
Max Magnitude0
ClinVar
Risk rs397516657(A;A)
Alt rs397516657(A;A)
Reference rs397516657(T;T)
Significance Probable-Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.68836316T>A
CLNSRC ClinVar
CLNACC RCV000037164.2,