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rs876657641

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657641(A;A)
Make rs876657641(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position70033470
GeneEDA
is asnp
is mentioned by
dbSNPrs876657641
ebirs876657641
HLIrs876657641
Exacrs876657641
Varsomers876657641
Maprs876657641
PheGenIrs876657641
hapmaprs876657641
1000 genomesrs876657641
hgdprs876657641
ensemblrs876657641
gopubmedrs876657641
geneviewrs876657641
scholarrs876657641
googlers876657641
pharmgkbrs876657641
gwascentralrs876657641
openSNPrs876657641
23andMers876657641
23andMe allrs876657641
SNP Nexus

SNPshotrs876657641
SNPdbers876657641
MSV3drs876657641
GWAS Ctlgrs876657641
Max Magnitude0
ClinVar
Risk rs876657641(A;A)
Alt rs876657641(A;A)
Reference rs876657641(G;G)
Significance Probable-Pathogenic
Disease Tooth agenesis
Variation info
Gene EDA
CLNDBN Tooth agenesis, selective, X-linked, 1
Reversed 0
HGVS NC_000023.10:g.69253320G>A
CLNSRC
CLNACC RCV000223248.1,