rs1135728
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs1135728(G;T) |
Make rs1135728(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 134143082 |
Gene | TCF7 |
is a | snp |
is | mentioned by |
dbSNP | rs1135728 |
dbSNP (classic) | rs1135728 |
ClinGen | rs1135728 |
ebi | rs1135728 |
HLI | rs1135728 |
Exac | rs1135728 |
Gnomad | rs1135728 |
Varsome | rs1135728 |
LitVar | rs1135728 |
Map | rs1135728 |
PheGenI | rs1135728 |
Biobank | rs1135728 |
1000 genomes | rs1135728 |
hgdp | rs1135728 |
ensembl | rs1135728 |
geneview | rs1135728 |
scholar | rs1135728 |
rs1135728 | |
pharmgkb | rs1135728 |
gwascentral | rs1135728 |
openSNP | rs1135728 |
23andMe | rs1135728 |
SNPshot | rs1135728 |
SNPdbe | rs1135728 |
MSV3d | rs1135728 |
GWAS Ctlg | rs1135728 |
Max Magnitude | 0 |
(Trp336Cys) in the HMG_box region of this gene is predicted to be deleterious by many methods (SIFT, env_score, SDM and Polyphen) [1]
[PMID 17708757] Genome bioinformatic analysis of nonsynonymous SNPs.