rs134136
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs134136(C;C) |
Make rs134136(C;T) |
Make rs134136(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 22 |
Position | 26503508 |
Gene | TFIP11 |
is a | snp |
is | mentioned by |
dbSNP | rs134136 |
dbSNP (classic) | rs134136 |
ClinGen | rs134136 |
ebi | rs134136 |
HLI | rs134136 |
Exac | rs134136 |
Gnomad | rs134136 |
Varsome | rs134136 |
LitVar | rs134136 |
Map | rs134136 |
PheGenI | rs134136 |
Biobank | rs134136 |
1000 genomes | rs134136 |
hgdp | rs134136 |
ensembl | rs134136 |
geneview | rs134136 |
scholar | rs134136 |
rs134136 | |
pharmgkb | rs134136 |
gwascentral | rs134136 |
openSNP | rs134136 |
23andMe | rs134136 |
SNPshot | rs134136 |
SNPdbe | rs134136 |
MSV3d | rs134136 |
GWAS Ctlg | rs134136 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 28382465] Significance of genetic variations in developmental enamel defects of primary dentition in Polish children.
[PMID 32945961] Genes in the pathway of tooth mineral tissues and dental caries risk: a systematic review and meta-analysis.