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rs397516676

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516676(-;-)
Make rs397516676(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position70033426
GeneEDA
is asnp
is mentioned by
dbSNPrs397516676
ebirs397516676
HLIrs397516676
Exacrs397516676
Varsomers397516676
Maprs397516676
PheGenIrs397516676
hapmaprs397516676
1000 genomesrs397516676
hgdprs397516676
ensemblrs397516676
gopubmedrs397516676
geneviewrs397516676
scholarrs397516676
googlers397516676
pharmgkbrs397516676
gwascentralrs397516676
openSNPrs397516676
23andMers397516676
23andMe allrs397516676
SNP Nexus

SNPshotrs397516676
SNPdbers397516676
MSV3drs397516676
GWAS Ctlgrs397516676
Max Magnitude0
ClinVar
Risk rs397516676(;)
Alt rs397516676(;)
Reference rs397516676(G;G)
Significance Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.69253276delG
CLNSRC ClinVar
CLNACC RCV000037188.2,