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Infertility and Recurrent Pregnancy Loss v0.194 | BNC1 | Zornitza Stark Marked gene: BNC1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Infertility and Recurrent Pregnancy Loss v0.194 | BNC1 | Zornitza Stark Gene: bnc1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Infertility and Recurrent Pregnancy Loss v0.194 | BNC1 | Zornitza Stark Classified gene: BNC1 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Infertility and Recurrent Pregnancy Loss v0.194 | BNC1 | Zornitza Stark Gene: bnc1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Infertility and Recurrent Pregnancy Loss v0.103 | BNC1 | Jasmine Chew edited their review of gene: BNC1: Changed publications: 32962729, 30010909, 39595984, 39462784 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Infertility and Recurrent Pregnancy Loss v0.103 | BNC1 |
Jasmine Chew changed review comment from: FeRGI database- Moderate evidence for POI- PMID:32962729,30010909 (Reported monoallelic and biallelic variants) Sources: Literature; to: FeRGI database- Moderate evidence for POI- PMID:32962729,30010909 (Reported monoallelic and biallelic variants) New papers reported monoallelic variants in POI patients- PMID: 39595984, 39462784 Sources: Literature |
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Infertility and Recurrent Pregnancy Loss v0.103 | BNC1 |
Jasmine Chew gene: BNC1 was added gene: BNC1 was added to Infertility and Pregnancy Loss. Sources: Literature Mode of inheritance for gene: BNC1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: BNC1 were set to 32962729; 30010909 Phenotypes for gene: BNC1 were set to Premature ovarian failure 16, MIM# 618723 Review for gene: BNC1 was set to GREEN Added comment: FeRGI database- Moderate evidence for POI- PMID:32962729,30010909 (Reported monoallelic and biallelic variants) Sources: Literature |