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rs876657639

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657639(C;T)
Make rs876657639(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position70035500
GeneEDA
is asnp
is mentioned by
dbSNPrs876657639
ebirs876657639
HLIrs876657639
Exacrs876657639
Varsomers876657639
Maprs876657639
PheGenIrs876657639
hapmaprs876657639
1000 genomesrs876657639
hgdprs876657639
ensemblrs876657639
gopubmedrs876657639
geneviewrs876657639
scholarrs876657639
googlers876657639
pharmgkbrs876657639
gwascentralrs876657639
openSNPrs876657639
23andMers876657639
23andMe allrs876657639
SNP Nexus

SNPshotrs876657639
SNPdbers876657639
MSV3drs876657639
GWAS Ctlgrs876657639
Max Magnitude0
ClinVar
Risk rs876657639(T;T)
Alt rs876657639(T;T)
Reference rs876657639(C;C)
Significance Probable-Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.69255350C>T
CLNSRC
CLNACC RCV000214858.1,