All individuals with variants in gene RUNX2

11 entries on 1 page. Showing entries 1 - 11.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00079877 - - - - - Germany - - - - - CCD - 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00117409 ? - - - - Argentina Latin American - - - - CCD cleidocranial dysplasia 1 1 Ariel I Suarez
00132208 - - - - - Germany - - - - - CCD - 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00163991 - - - - - - - - - - - CCD - 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00219179 - - - ? - - - - - - - ? HP:0002652 (Skeletal dysplasia) 1 1 IMGAG
00229652 - - - F - - - - - - - ? Global developmental delay (HP:0001263); Short stature (HP:0004322) 1 1 IMGAG
00294123 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 8 Mohammed Faruq
00359447 - - - - - (Brazil) - - - - - CCD - 1 1 Cynthia Silveira
00359448 - - - - - (Brazil) - - - - - CCD - 1 1 Cynthia Silveira
00359453 - - - - - (Brazil) - - - - - CCD - 1 1 Cynthia Silveira
00455332 - - - F - - (not applicable) white - - - - ? HP:0006660, HP:0004322, HP:0000164, HP:0011069, HP:0002007, HP:0000670, HP:0002650, HP:0005773, HP:0005736, HP:0000316, HP:0000248, HP:0001591 1 1 Marketa Wayhelova
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