rs755155385
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TATT;TATT) | 0 | common/normal |
Make rs755155385(-;-) |
Make rs755155385(-;TATT) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 4 |
Position | 99591636 |
Gene | MTTP |
is a | snp |
is | mentioned by |
dbSNP | rs755155385 |
dbSNP (classic) | rs755155385 |
ClinGen | rs755155385 |
ebi | rs755155385 |
HLI | rs755155385 |
Exac | rs755155385 |
Gnomad | rs755155385 |
Varsome | rs755155385 |
LitVar | rs755155385 |
Map | rs755155385 |
PheGenI | rs755155385 |
Biobank | rs755155385 |
1000 genomes | rs755155385 |
hgdp | rs755155385 |
ensembl | rs755155385 |
geneview | rs755155385 |
scholar | rs755155385 |
rs755155385 | |
pharmgkb | rs755155385 |
gwascentral | rs755155385 |
openSNP | rs755155385 |
23andMe | rs755155385 |
SNPshot | rs755155385 |
SNPdbe | rs755155385 |
MSV3d | rs755155385 |
GWAS Ctlg | rs755155385 |
Max Magnitude | 0 |
Non-coding variant assessed as part of Blueprint Genetics Retinal dystrophy (266 gene) panel.