DONSON Chromosome 21
DNA replication fork stabilization factor DONSON
Upload your DNA to see your personal genotypes for variants in DONSON.
What This Gene Does
This gene lies downstream of the SON gene and spans 10 kb on chromosome 21. The function of this gene is unknown. [provided by RefSeq, Jul 2008]
Associated Conditions (11)
DONSON-related Meier-Gorlin syndrome
Meier-Gorlin syndrome
Microcephaly
short stature
and limb abnormalities
Microcephaly-micromelia syndrome
DONSON-related disorder
Inborn genetic diseases
See cases
Ovarian serous cystadenocarcinoma
Meier-Gorlin syndrome 1
Key Variants
RS1028163227
Conflicting classifications of pathogenicity
DONSON-related Meier-Gorlin syndrome, Meier-Gorlin syndrome, Microcephaly
Health Risk
RS1135401960
Conflicting classifications of pathogenicity
Microcephaly, short stature, and limb abnormalities
Health Risk
RS140592434
Conflicting classifications of pathogenicity
DONSON-related disorder, DONSON-related disorder
Health Risk
RS146664036
Conflicting classifications of pathogenicity
Inborn genetic diseases, Microcephaly-micromelia syndrome, Microcephaly
Health Risk
RS147415181
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS202168282
Conflicting classifications of pathogenicity
DONSON-related disorder, DONSON-related disorder
Health Risk
RS367904759
Conflicting classifications of pathogenicity
DONSON-related Meier-Gorlin syndrome, Meier-Gorlin syndrome, DONSON-related Meier-Gorlin syndrome
Health Risk
RS544638959
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS61746119
Conflicting classifications of pathogenicity
Health Risk
RS766593943
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS768071555
Conflicting classifications of pathogenicity
Inborn genetic diseases, Microcephaly-micromelia syndrome, Microcephaly
Health Risk
RS2086519334
Likely pathogenic
Health Risk
All Variants (45)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS1028163227 | Health Risk | Conflicting classifications of pathogenicity | DONSON-related Meier-Gorlin syndrome, Meier-Gorlin syndrome, Microcephaly |
| RS1135401960 | Health Risk | Conflicting classifications of pathogenicity | Microcephaly, short stature, and limb abnormalities |
| RS140592434 | Health Risk | Conflicting classifications of pathogenicity | DONSON-related disorder, DONSON-related disorder |
| RS146664036 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Microcephaly-micromelia syndrome, Microcephaly |
| RS147415181 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS202168282 | Health Risk | Conflicting classifications of pathogenicity | DONSON-related disorder, DONSON-related disorder |
| RS367904759 | Health Risk | Conflicting classifications of pathogenicity | DONSON-related Meier-Gorlin syndrome, Meier-Gorlin syndrome, DONSON-related Meier-Gorlin syndrome |
| RS544638959 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS61746119 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS766593943 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS768071555 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Microcephaly-micromelia syndrome, Microcephaly |
| RS2086519334 | Health Risk | Likely pathogenic | — |
| RS2517470416 | Health Risk | Likely pathogenic | Microcephaly, short stature, and limb abnormalities |
| RS2517474861 | Health Risk | Likely pathogenic | Microcephaly, short stature, and limb abnormalities |
| RS2517484911 | Health Risk | Likely pathogenic | — |
| RS534299298 | Health Risk | Likely pathogenic | Microcephaly, short stature, and limb abnormalities |
| RS762881899 | Health Risk | Likely pathogenic | — |
| RS779803447 | Health Risk | Likely pathogenic | Microcephaly, short stature, and limb abnormalities |
| RS1135401959 | Health Risk | Pathogenic | Microcephaly, short stature, and limb abnormalities |
| RS1135401961 | Health Risk | Pathogenic | Microcephaly, short stature, and limb abnormalities |
| RS1165425393 | Health Risk | Pathogenic | — |
| RS1247764954 | Health Risk | Pathogenic | — |
| RS1354181982 | Health Risk | Pathogenic | — |
| RS1450835871 | Health Risk | Pathogenic | — |
| RS1468284861 | Health Risk | Pathogenic | — |
| RS2086478717 | Health Risk | Pathogenic | — |
| RS2145899336 | Health Risk | Pathogenic | — |
| RS2517474921 | Health Risk | Pathogenic | Inborn genetic diseases, Inborn genetic diseases |
| RS2517484685 | Health Risk | Pathogenic | Microcephaly, short stature, and limb abnormalities |
| RS372126686 | Health Risk | Pathogenic | — |
| RS542296982 | Health Risk | Pathogenic | DONSON-related disorder, DONSON-related disorder |
| RS748118576 | Health Risk | Pathogenic | — |
| RS752810960 | Health Risk | Pathogenic | Meier-Gorlin syndrome, Meier-Gorlin syndrome |
| RS753648048 | Health Risk | Pathogenic | Inborn genetic diseases, Inborn genetic diseases |
| RS760760475 | Health Risk | Pathogenic | — |
| RS774052186 | Health Risk | Pathogenic | Meier-Gorlin syndrome, Meier-Gorlin syndrome |
| RS774616573 | Health Risk | Pathogenic | Meier-Gorlin syndrome, Meier-Gorlin syndrome |
| RS775673237 | Health Risk | Pathogenic | — |
| RS777061964 | Health Risk | Pathogenic | Microcephaly, short stature, and limb abnormalities |
| RS779149681 | Health Risk | Pathogenic | Microcephaly, short stature, and limb abnormalities |
| RS990508855 | Health Risk | Pathogenic | See cases, See cases |
| RS1010722195 | Health Risk | Pathogenic/Likely pathogenic | Meier-Gorlin syndrome, Microcephaly, short stature |
| RS2145910302 | Health Risk | Pathogenic/Likely pathogenic | Meier-Gorlin syndrome 1, Meier-Gorlin syndrome 1 |
| RS765112107 | Health Risk | Pathogenic/Likely pathogenic | Inborn genetic diseases, Microcephaly, short stature |
| RS993687029 | Health Risk | Pathogenic/Likely pathogenic | Microcephaly, short stature, and limb abnormalities |