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rs397516654

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516654(C;C)
Make rs397516654(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position70035527
GeneEDA
is asnp
is mentioned by
dbSNPrs397516654
ebirs397516654
HLIrs397516654
Exacrs397516654
Varsomers397516654
Maprs397516654
PheGenIrs397516654
hapmaprs397516654
1000 genomesrs397516654
hgdprs397516654
ensemblrs397516654
gopubmedrs397516654
geneviewrs397516654
scholarrs397516654
googlers397516654
pharmgkbrs397516654
gwascentralrs397516654
openSNPrs397516654
23andMers397516654
23andMe allrs397516654
SNP Nexus

SNPshotrs397516654
SNPdbers397516654
MSV3drs397516654
GWAS Ctlgrs397516654
Max Magnitude0
ClinVar
Risk rs397516654(C;C)
Alt rs397516654(C;C)
Reference rs397516654(T;T)
Significance Probable-Pathogenic
Disease Tooth agenesis
Variation info
Gene EDA
CLNDBN Tooth agenesis, selective, X-linked, 1
Reversed 0
HGVS NC_000023.10:g.69255377T>C
CLNSRC ClinVar
CLNACC RCV000037161.2,