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| Spontaneous coronary artery dissection v0.51 | YY1AP1 | Zornitza Stark reviewed gene: YY1AP1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Grange syndrome, MIM# 602531; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Spontaneous coronary artery dissection v0.48 | YY1AP1 | Ain Roesley Publications for gene: YY1AP1 were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Spontaneous coronary artery dissection v0.47 | YY1AP1 | Ain Roesley Classified gene: YY1AP1 as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Spontaneous coronary artery dissection v0.47 | YY1AP1 | Ain Roesley Gene: yy1ap1 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Spontaneous coronary artery dissection v0.46 | YY1AP1 | Ain Roesley edited their review of gene: YY1AP1: Changed rating: AMBER; Changed publications: 33125268 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Spontaneous coronary artery dissection v0.46 | YY1AP1 |
Ain Roesley changed review comment from: PMID: 33125268 1x individual with a canonical splice + 1x protein truncating variant. However, phasing could not be performed no other literature found Sources: Literature; to: PMID: 33125268 1x individual with a canonical splice + 1x protein truncating variant. However, phasing could not be performed no other literature found amber so as to not miss a diagnosis Sources: Literature |
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| Spontaneous coronary artery dissection v0.46 | YY1AP1 |
Ain Roesley changed review comment from: PMID: 37979122; listed as "likely monogenic disease effect" PMID: 33125268 was cited in paper above. 1x individual with a canonical splice + 1x protein truncating variant. However, phasing could not be performed no other literature found Sources: Literature; to: PMID: 33125268 1x individual with a canonical splice + 1x protein truncating variant. However, phasing could not be performed no other literature found Sources: Literature |
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| Spontaneous coronary artery dissection v0.32 | YY1AP1 | Ain Roesley Marked gene: YY1AP1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Spontaneous coronary artery dissection v0.32 | YY1AP1 | Ain Roesley Gene: yy1ap1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Spontaneous coronary artery dissection v0.32 | YY1AP1 | Ain Roesley edited their review of gene: YY1AP1: Changed publications: 37979122, 33125268 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Spontaneous coronary artery dissection v0.32 | YY1AP1 |
Ain Roesley gene: YY1AP1 was added gene: YY1AP1 was added to Spontaneous coronary artery dissection. Sources: Literature Mode of inheritance for gene: YY1AP1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: YY1AP1 were set to Grange syndrome, MIM# 602531 Review for gene: YY1AP1 was set to RED gene: YY1AP1 was marked as current diagnostic Added comment: PMID: 37979122; listed as "likely monogenic disease effect" PMID: 33125268 was cited in paper above. 1x individual with a canonical splice + 1x protein truncating variant. However, phasing could not be performed no other literature found Sources: Literature |
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