FOCAD Chromosome 9
Focadhesin
Upload your DNA to see your personal genotypes for variants in FOCAD.
What This Gene Does
Predicted to be involved in regulation of post-transcriptional gene silencing. Located in cytosol and focal adhesion. [provided by Alliance of Genome Resources, Jul 2025]
Gene Info
Gene Group
"Armadillo like helical domain containing|MicroRNA protein coding host genes|Small nucleolar RNA protein coding host genes"
Locus Type
gene with protein product
Location
9p21.3
Ensembl
ENSG00000188352
Associated Conditions (6)
Inborn genetic diseases
FOCAD-related disorder
Cervical cancer
Gastric cancer
Liver disease
severe congenital
Key Variants
RS140318156
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS140435235
Conflicting classifications of pathogenicity
FOCAD-related disorder, Inborn genetic diseases, FOCAD-related disorder
Health Risk
RS141558162
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS141572748
Conflicting classifications of pathogenicity
Inborn genetic diseases, FOCAD-related disorder, Inborn genetic diseases
Health Risk
RS144110783
Conflicting classifications of pathogenicity
FOCAD-related disorder, Inborn genetic diseases, FOCAD-related disorder
Health Risk
RS148407192
Conflicting classifications of pathogenicity
FOCAD-related disorder, Inborn genetic diseases, FOCAD-related disorder
Health Risk
RS148495154
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS148685443
Conflicting classifications of pathogenicity
Inborn genetic diseases, FOCAD-related disorder, Inborn genetic diseases
Health Risk
RS149760366
Conflicting classifications of pathogenicity
Inborn genetic diseases, Cervical cancer, Gastric cancer
Health Risk
RS187249342
Conflicting classifications of pathogenicity
Inborn genetic diseases, FOCAD-related disorder, Inborn genetic diseases
Health Risk
RS551102582
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS755212646
Conflicting classifications of pathogenicity
Health Risk
All Variants (19)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS140318156 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS140435235 | Health Risk | Conflicting classifications of pathogenicity | FOCAD-related disorder, Inborn genetic diseases, FOCAD-related disorder |
| RS141558162 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS141572748 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, FOCAD-related disorder, Inborn genetic diseases |
| RS144110783 | Health Risk | Conflicting classifications of pathogenicity | FOCAD-related disorder, Inborn genetic diseases, FOCAD-related disorder |
| RS148407192 | Health Risk | Conflicting classifications of pathogenicity | FOCAD-related disorder, Inborn genetic diseases, FOCAD-related disorder |
| RS148495154 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS148685443 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, FOCAD-related disorder, Inborn genetic diseases |
| RS149760366 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Cervical cancer, Gastric cancer |
| RS187249342 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, FOCAD-related disorder, Inborn genetic diseases |
| RS551102582 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS755212646 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS1834683448 | Health Risk | Likely pathogenic | Liver disease, severe congenital, Liver disease |
| RS1161907698 | Health Risk | Pathogenic | Liver disease, severe congenital, Liver disease |
| RS1481004397 | Health Risk | Pathogenic | Liver disease, severe congenital, Liver disease |
| RS1833052702 | Health Risk | Pathogenic | Liver disease, severe congenital, Liver disease |
| RS200873740 | Health Risk | Pathogenic | Liver disease, severe congenital, Liver disease |
| RS2132603627 | Health Risk | Pathogenic | Liver disease, severe congenital, Liver disease |
| RS2492625531 | Health Risk | Pathogenic | — |