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rs397516672

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516672(C;T)
Make rs397516672(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position70029527
GeneEDA
is asnp
is mentioned by
dbSNPrs397516672
ebirs397516672
HLIrs397516672
Exacrs397516672
Varsomers397516672
Maprs397516672
PheGenIrs397516672
hapmaprs397516672
1000 genomesrs397516672
hgdprs397516672
ensemblrs397516672
gopubmedrs397516672
geneviewrs397516672
scholarrs397516672
googlers397516672
pharmgkbrs397516672
gwascentralrs397516672
openSNPrs397516672
23andMers397516672
23andMe allrs397516672
SNP Nexus

SNPshotrs397516672
SNPdbers397516672
MSV3drs397516672
GWAS Ctlgrs397516672
Max Magnitude0
ClinVar
Risk rs397516672(T;T)
Alt rs397516672(T;T)
Reference rs397516672(C;C)
Significance Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.69249377C>T
CLNSRC ClinVar
CLNACC RCV000037183.3,