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rs397516677

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516677(A;A)
Make rs397516677(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position70033475
GeneEDA
is asnp
is mentioned by
dbSNPrs397516677
ebirs397516677
HLIrs397516677
Exacrs397516677
Varsomers397516677
Maprs397516677
PheGenIrs397516677
hapmaprs397516677
1000 genomesrs397516677
hgdprs397516677
ensemblrs397516677
gopubmedrs397516677
geneviewrs397516677
scholarrs397516677
googlers397516677
pharmgkbrs397516677
gwascentralrs397516677
openSNPrs397516677
23andMers397516677
23andMe allrs397516677
SNP Nexus

SNPshotrs397516677
SNPdbers397516677
MSV3drs397516677
GWAS Ctlgrs397516677
Max Magnitude0
ClinVar
Risk rs397516677(A;A)
Alt rs397516677(A;A)
Reference rs397516677(G;G)
Significance Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.69253325G>A
CLNSRC ClinVar
CLNACC RCV000037189.2,