DONSON Chromosome 21

DNA replication fork stabilization factor DONSON
45 variants 45 Health Risk

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
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
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