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rs397516656

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397516656(-;-)
Make rs397516656(-;G)
Make rs397516656(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position69616580
GeneEDA
is asnp
is mentioned by
dbSNPrs397516656
ebirs397516656
HLIrs397516656
Exacrs397516656
Varsomers397516656
Maprs397516656
PheGenIrs397516656
hapmaprs397516656
1000 genomesrs397516656
hgdprs397516656
ensemblrs397516656
gopubmedrs397516656
geneviewrs397516656
scholarrs397516656
googlers397516656
pharmgkbrs397516656
gwascentralrs397516656
openSNPrs397516656
23andMers397516656
23andMe allrs397516656
SNP Nexus

SNPshotrs397516656
SNPdbers397516656
MSV3drs397516656
GWAS Ctlgrs397516656
Max Magnitude0
ClinVar
Risk rs397516656(G;G)
Alt rs397516656(G;G)
Reference rs397516656(;)
Significance Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.68836424dupG
CLNSRC ClinVar
CLNACC RCV000037163.2,