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rs132630319

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs132630319(C;G)
Make rs132630319(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position69616501
GeneEDA
is asnp
is mentioned by
dbSNPrs132630319
ebirs132630319
HLIrs132630319
Exacrs132630319
Varsomers132630319
Maprs132630319
PheGenIrs132630319
hapmaprs132630319
1000 genomesrs132630319
hgdprs132630319
ensemblrs132630319
gopubmedrs132630319
geneviewrs132630319
scholarrs132630319
googlers132630319
pharmgkbrs132630319
gwascentralrs132630319
openSNPrs132630319
23andMers132630319
23andMe allrs132630319
SNP Nexus

SNPshotrs132630319
SNPdbers132630319
MSV3drs132630319
GWAS Ctlgrs132630319
Max Magnitude0
OMIM300451
Desc
Variant0014
Relatedalso
ClinVar
Risk rs132630319(G;G)
Alt rs132630319(G;G)
Reference rs132630319(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.68836345C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000011791.9,