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rs397516662

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516662(C;T)
Make rs397516662(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position69957087
GeneEDA
is asnp
is mentioned by
dbSNPrs397516662
ebirs397516662
HLIrs397516662
Exacrs397516662
Varsomers397516662
Maprs397516662
PheGenIrs397516662
hapmaprs397516662
1000 genomesrs397516662
hgdprs397516662
ensemblrs397516662
gopubmedrs397516662
geneviewrs397516662
scholarrs397516662
googlers397516662
pharmgkbrs397516662
gwascentralrs397516662
openSNPrs397516662
23andMers397516662
23andMe allrs397516662
SNP Nexus

SNPshotrs397516662
SNPdbers397516662
MSV3drs397516662
GWAS Ctlgrs397516662
Max Magnitude0
ClinVar
Risk rs397516662(T;T)
Alt rs397516662(T;T)
Reference rs397516662(C;C)
Significance Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.69176937C>T
CLNSRC ClinVar
CLNACC RCV000037169.3,