All individuals with variants in gene COL9A1

13 entries on 1 page. Showing entries 1 - 13.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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VIP     

Data_av     

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Phenotype details     

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Owner     
00207702 - - - F yes United Kingdom (Great Britain) - - - - - STL4 Congenital sensorineural hyearing loss High myopia Hypoplastic vitreous gel 1 1 Thomas Nixon
00235307 E26 PubMed: Hofrichter 2019 - M no Iran - - - - - DFNB Apparent non-syndromic hearing loss with no other signs of a syndrome. 1 2 Barbara Vona
00248523 - - proband and affected mother - - - - - - - - EDM2 - 1 2 LOVD
00248524 - - 4 affected sibs, parents heterozygous carriers - yes Morocco - - - - - STL4 - 1 5 LOVD
00294174 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 209 Mohammed Faruq
00294175 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 5 Mohammed Faruq
00294176 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 9 Mohammed Faruq
00294177 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00305113 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 7 Mohammed Faruq
00358950 Case71876 PubMed: Tiwari 2016 see paper F - Switzerland - - - - - retinal disease see paper; ... 1 1 LOVD
00358967 Case71315 PubMed: Tiwari 2016 see paper M - Switzerland - - - - - retinal disease see paper; ... 1 1 LOVD
00358979 Case71808 PubMed: Tiwari 2016 see paper M - Switzerland - - - - - retinal disease see paper; ... 1 1 LOVD
00386879 121-246 PubMed: Zampaglione 2020 - ? - - - - - - - retinal disease - 1 1 LOVD
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