The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes
PMID: 28600779
Gene: ABCA4
HGNCID: HGNC:34
MonDO:
Case: 16N-0520, Male, Saudi Arabia, 1 yo
DiseaseAssertion:
FamilyInfo: Consanguineous parents, positive family history
CasePresentingHPOs: HP:0000618, HP:0000648 (Blindness, Optic atrophy)
CaseHPOFreeText: Coloboma of eye
GenotypingMethod: WES, analysis of Vision Panel, constituent genes are described in PMID 26112015.
SupplementalData: Supplemental table
Variant: ABCA4:NM_000350:exon49:c.6764G>T:p.S2255I
CAID: CA202970
gnomAD: 0.4845 (gnomAD v4.0.0, Grpmax Filtered AF African/African-American) https://gnomad.broadinstitute.org/variant/1-93996161-C-A?dataset=gnomad_r4
VariantEvidence: Authors classified as VOUS. But later downgraded to LB in PMID 31130284.