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rs2278163

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2278163(C;T)
Make rs2278163(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position49995062
GeneDLX3
is asnp
is mentioned by
dbSNPrs2278163
dbSNP (classic)rs2278163
ClinGenrs2278163
ebirs2278163
HLIrs2278163
Exacrs2278163
Gnomadrs2278163
Varsomers2278163
LitVarrs2278163
Maprs2278163
PheGenIrs2278163
Biobankrs2278163
1000 genomesrs2278163
hgdprs2278163
ensemblrs2278163
geneviewrs2278163
scholarrs2278163
googlers2278163
pharmgkbrs2278163
gwascentralrs2278163
openSNPrs2278163
23andMers2278163
SNPshotrs2278163
SNPdbers2278163
MSV3drs2278163
GWAS Ctlgrs2278163
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 25247779] Association of DLX3 gene polymorphism and dental caries susceptibility in Japanese children


ClinVar
Risk rs2278163(T;T)
Alt rs2278163(T;T)
Reference Rs2278163(C;C)
Significance Non-pathogenic
Disease Amelogenesis Imperfecta
Variation info
Gene DLX3
CLNDBN Amelogenesis Imperfecta, Dominant
Reversed 1
HGVS NC_000017.10:g.48072426G>A
CLNSRC
CLNACC RCV000404262.1,