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rs876657687

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876657687(G;G)
Make rs876657687(G;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position70035393
GeneEDA
is asnp
is mentioned by
dbSNPrs876657687
ebirs876657687
HLIrs876657687
Exacrs876657687
Varsomers876657687
Maprs876657687
PheGenIrs876657687
hapmaprs876657687
1000 genomesrs876657687
hgdprs876657687
ensemblrs876657687
gopubmedrs876657687
geneviewrs876657687
scholarrs876657687
googlers876657687
pharmgkbrs876657687
gwascentralrs876657687
openSNPrs876657687
23andMers876657687
23andMe allrs876657687
SNP Nexus

SNPshotrs876657687
SNPdbers876657687
MSV3drs876657687
GWAS Ctlgrs876657687
Max Magnitude0
ClinVar
Risk rs876657687(G;G)
Alt rs876657687(G;G)
Reference rs876657687(T;T)
Significance Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.69255243T>G
CLNSRC
CLNACC RCV000222108.1,