rs2278163
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2278163(C;T) |
Make rs2278163(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 49995062 |
Gene | DLX3 |
is a | snp |
is | mentioned by |
dbSNP | rs2278163 |
dbSNP (classic) | rs2278163 |
ClinGen | rs2278163 |
ebi | rs2278163 |
HLI | rs2278163 |
Exac | rs2278163 |
Gnomad | rs2278163 |
Varsome | rs2278163 |
LitVar | rs2278163 |
Map | rs2278163 |
PheGenI | rs2278163 |
Biobank | rs2278163 |
1000 genomes | rs2278163 |
hgdp | rs2278163 |
ensembl | rs2278163 |
geneview | rs2278163 |
scholar | rs2278163 |
rs2278163 | |
pharmgkb | rs2278163 |
gwascentral | rs2278163 |
openSNP | rs2278163 |
23andMe | rs2278163 |
SNPshot | rs2278163 |
SNPdbe | rs2278163 |
MSV3d | rs2278163 |
GWAS Ctlg | rs2278163 |
Max Magnitude | 0 |
? | (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, |