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rs876657640

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876657640(A;T)
Make rs876657640(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position69957107
GeneEDA
is asnp
is mentioned by
dbSNPrs876657640
ebirs876657640
HLIrs876657640
Exacrs876657640
Varsomers876657640
Maprs876657640
PheGenIrs876657640
hapmaprs876657640
1000 genomesrs876657640
hgdprs876657640
ensemblrs876657640
gopubmedrs876657640
geneviewrs876657640
scholarrs876657640
googlers876657640
pharmgkbrs876657640
gwascentralrs876657640
openSNPrs876657640
23andMers876657640
23andMe allrs876657640
SNP Nexus

SNPshotrs876657640
SNPdbers876657640
MSV3drs876657640
GWAS Ctlgrs876657640
Max Magnitude0
ClinVar
Risk rs876657640(T;T)
Alt rs876657640(T;T)
Reference rs876657640(A;A)
Significance Probable-Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.69176957A>T
CLNSRC
CLNACC RCV000218495.1,