All individuals with variants in gene OPN1MW

10 entries on 1 page. Showing entries 1 - 10.
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AscendingIndividual ID     

ID_report     

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VIP     

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Owner     
00183137 25644381-FamAU29 PubMed: Hu 2016 family, 2 affected, 1 unaffected heterozygous carrier female M - - - - - - - MRX;IDX - 1 2 Johan den Dunnen
00309272 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00309274 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00309275 - PubMed: Sharon 2019 6 IRD families - - Israel - - - - - retinal disease - 1 6 Global Variome, with Curator vacancy
00309278 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00387638 26 PubMed: Zanolli 2020 individual ID not present in paper, consecutive numbers given ? - Chile - - - - - retinal disease - 1 1 LOVD
00447026 BCM-308-1 PubMed: Weisschuh 2024 family, 2 affected M - Germany - - - - - ? - 1 2 Johan den Dunnen
00447120 CRD-844-1 PubMed: Weisschuh 2024 family, >3 affected F - Germany - - - - - ? - 1 4 Johan den Dunnen
00447121 CRD-844-2 PubMed: Weisschuh 2024 relative M - Germany - - - - - ? - 1 1 Johan den Dunnen
00447369 STGD-408 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - ? - 1 1 Johan den Dunnen
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