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

rs397516659

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516659(C;C)
Make rs397516659(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position69616310
GeneEDA
is asnp
is mentioned by
dbSNPrs397516659
ebirs397516659
HLIrs397516659
Exacrs397516659
Varsomers397516659
Maprs397516659
PheGenIrs397516659
hapmaprs397516659
1000 genomesrs397516659
hgdprs397516659
ensemblrs397516659
gopubmedrs397516659
geneviewrs397516659
scholarrs397516659
googlers397516659
pharmgkbrs397516659
gwascentralrs397516659
openSNPrs397516659
23andMers397516659
23andMe allrs397516659
SNP Nexus

SNPshotrs397516659
SNPdbers397516659
MSV3drs397516659
GWAS Ctlgrs397516659
Max Magnitude0
ClinVar
Risk rs397516659(C;C)
Alt rs397516659(C;C)
Reference rs397516659(T;T)
Significance Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.68836154T>C
CLNSRC ClinVar
CLNACC RCV000037166.2,