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rs397516661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516661(A;A)
Make rs397516661(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position69616655
GeneEDA
is asnp
is mentioned by
dbSNPrs397516661
ebirs397516661
HLIrs397516661
Exacrs397516661
Varsomers397516661
Maprs397516661
PheGenIrs397516661
hapmaprs397516661
1000 genomesrs397516661
hgdprs397516661
ensemblrs397516661
gopubmedrs397516661
geneviewrs397516661
scholarrs397516661
googlers397516661
pharmgkbrs397516661
gwascentralrs397516661
openSNPrs397516661
23andMers397516661
23andMe allrs397516661
SNP Nexus

SNPshotrs397516661
SNPdbers397516661
MSV3drs397516661
GWAS Ctlgrs397516661
Max Magnitude0
ClinVar
Risk rs397516661(A;A)
Alt rs397516661(A;A)
Reference rs397516661(T;T)
Significance Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.68836499T>A
CLNSRC ClinVar
CLNACC RCV000037168.2,