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rs142948132

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs142948132(A;A)
Make rs142948132(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position70035434
GeneEDA
is asnp
is mentioned by
dbSNPrs142948132
ebirs142948132
HLIrs142948132
Exacrs142948132
Varsomers142948132
Maprs142948132
PheGenIrs142948132
hapmaprs142948132
1000 genomesrs142948132
hgdprs142948132
ensemblrs142948132
gopubmedrs142948132
geneviewrs142948132
scholarrs142948132
googlers142948132
pharmgkbrs142948132
gwascentralrs142948132
openSNPrs142948132
23andMers142948132
23andMe allrs142948132
SNP Nexus

SNPshotrs142948132
SNPdbers142948132
MSV3drs142948132
GWAS Ctlgrs142948132
Max Magnitude0
ClinVar
Risk rs142948132(A;A)
Alt rs142948132(A;A)
Reference rs142948132(G;G)
Significance Pathogenic
Disease Tooth agenesis not specified
Variation info
Gene EDA
CLNDBN Tooth agenesis, selective, X-linked, 1 not specified
Reversed 0
HGVS NC_000023.10:g.69255284G>A; NC_000023.10:g.69255284G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000239557.1, RCV000223353.1,