rs758966293
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs758966293(C;T) |
Make rs758966293(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 126275377 |
Gene | FOXRED1 |
is a | snp |
is | mentioned by |
dbSNP | rs758966293 |
dbSNP (classic) | rs758966293 |
ClinGen | rs758966293 |
ebi | rs758966293 |
HLI | rs758966293 |
Exac | rs758966293 |
Gnomad | rs758966293 |
Varsome | rs758966293 |
LitVar | rs758966293 |
Map | rs758966293 |
PheGenI | rs758966293 |
Biobank | rs758966293 |
1000 genomes | rs758966293 |
hgdp | rs758966293 |
ensembl | rs758966293 |
geneview | rs758966293 |
scholar | rs758966293 |
rs758966293 | |
pharmgkb | rs758966293 |
gwascentral | rs758966293 |
openSNP | rs758966293 |
23andMe | rs758966293 |
SNPshot | rs758966293 |
SNPdbe | rs758966293 |
MSV3d | rs758966293 |
GWAS Ctlg | rs758966293 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs758966293(T;T) |
Alt | rs758966293(T;T) |
Reference | Rs758966293(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | FOXRED1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.126145272C>T |
CLNSRC | |
CLNACC | RCV000195921.1, |