rs17089925
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17089925(C;C) |
Make rs17089925(C;T) |
Make rs17089925(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 55733603 |
Gene | LOC105372130 |
is a | snp |
is | mentioned by |
dbSNP | rs17089925 |
dbSNP (classic) | rs17089925 |
ClinGen | rs17089925 |
ebi | rs17089925 |
HLI | rs17089925 |
Exac | rs17089925 |
Gnomad | rs17089925 |
Varsome | rs17089925 |
LitVar | rs17089925 |
Map | rs17089925 |
PheGenI | rs17089925 |
Biobank | rs17089925 |
1000 genomes | rs17089925 |
hgdp | rs17089925 |
ensembl | rs17089925 |
geneview | rs17089925 |
scholar | rs17089925 |
rs17089925 | |
pharmgkb | rs17089925 |
gwascentral | rs17089925 |
openSNP | rs17089925 |
23andMe | rs17089925 |
SNPshot | rs17089925 |
SNPdbe | rs17089925 |
MSV3d | rs17089925 |
GWAS Ctlg | rs17089925 |
GMAF | 0.1538 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
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[PMID 21659310] Association of TCF4 Gene Polymorphisms with Fuchs Corneal Dystrophy in the Chinese