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| Genomic imprinting v0.131 | SNRPN | Sarah Leigh Classified gene: SNRPN as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic imprinting v0.131 | SNRPN | Sarah Leigh Gene: snrpn has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic imprinting v0.130 | SNRPN | Sarah Leigh Publications for gene: SNRPN were set to 30794780; http://igc.otago.ac.nz/home.html | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic imprinting v0.129 | SNRPN | Sarah Leigh edited their review of gene: SNRPN: Added comment: Associated with relevant phenotype in OMIM and as definitive Gen2Phen gene. Numerous cases of variants, including deletions of SNRPN have been reported (PMID: 29437285;34200226;34099539).; Changed rating: GREEN; Changed publications to: 29437285, 34200226, 34099539 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic imprinting v0.108 | SNRPN | Sarah Leigh Phenotypes for gene: SNRPN were changed from to Prader-Willi syndrome, OMIM:176270 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic imprinting v0.26 | SNRPN | Sarah Leigh reviewed gene: SNRPN: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic imprinting v0.24 | SNRPN |
Sarah Leigh gene: SNRPN was added gene: SNRPN was added to Imprinted Genes. Sources: Literature Mode of inheritance for gene: SNRPN was set to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed) Publications for gene: SNRPN were set to 30794780; http://igc.otago.ac.nz/home.html |
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