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rs397516682

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516682(G;T)
Make rs397516682(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position70035394
GeneEDA
is asnp
is mentioned by
dbSNPrs397516682
ebirs397516682
HLIrs397516682
Exacrs397516682
Varsomers397516682
Maprs397516682
PheGenIrs397516682
hapmaprs397516682
1000 genomesrs397516682
hgdprs397516682
ensemblrs397516682
gopubmedrs397516682
geneviewrs397516682
scholarrs397516682
googlers397516682
pharmgkbrs397516682
gwascentralrs397516682
openSNPrs397516682
23andMers397516682
23andMe allrs397516682
SNP Nexus

SNPshotrs397516682
SNPdbers397516682
MSV3drs397516682
GWAS Ctlgrs397516682
Max Magnitude0
ClinVar
Risk rs397516682(T;T)
Alt rs397516682(T;T)
Reference rs397516682(G;G)
Significance Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.69255244G>T
CLNSRC ClinVar
CLNACC RCV000037194.2,