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rs879255551

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879255551(C;T)
Make rs879255551(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position70033469
GeneEDA
is asnp
is mentioned by
dbSNPrs879255551
ebirs879255551
HLIrs879255551
Exacrs879255551
Varsomers879255551
Maprs879255551
PheGenIrs879255551
hapmaprs879255551
1000 genomesrs879255551
hgdprs879255551
ensemblrs879255551
gopubmedrs879255551
geneviewrs879255551
scholarrs879255551
googlers879255551
pharmgkbrs879255551
gwascentralrs879255551
openSNPrs879255551
23andMers879255551
23andMe allrs879255551
SNP Nexus

SNPshotrs879255551
SNPdbers879255551
MSV3drs879255551
GWAS Ctlgrs879255551
Max Magnitude0
ClinVar
Risk rs879255551(T;T)
Alt rs879255551(T;T)
Reference rs879255551(C;C)
Significance Pathogenic
Disease Tooth agenesis
Variation info
Gene EDA
CLNDBN Tooth agenesis, selective, X-linked, 1
Reversed 0
HGVS NC_000023.10:g.69253319C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000239506.1,