All genomic variants

8 entries on 1 page. Showing entries 1 - 8.
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Variant ID     

Effect     

Chr     

AscendingDNA change (genomic) (hg38)     

Reference     

DB-ID     

Frequency     

Allele Count     

Allele Number     

Owner     
0000000255 ./. 1 g.23750961C>T dbSNP chr1_000003 0.119 Control 84 704 Admin
0000000760 ./. 1 g.23750961C>T dbSNP chr1_000003 0.500 Patients_Q37.0 1 2 Admin
0000001080 ./. 1 g.23750961C>T dbSNP chr1_000003 0.250 Patients_Q37.3_left 1 4 Admin
0000001250 ./. 1 g.23750961C>T dbSNP chr1_000003 0.333 Patients_Q37.3_right 2 6 Admin
0000001454 ./. 1 g.23750961C>T dbSNP chr1_000003 0.179 Patients_Q37.4 19 106 Admin
0000001886 ./. 1 g.23750961C>T dbSNP chr1_000003 0.181 Patients_Q37.5_left 21 116 Admin
0000002139 ./. 1 g.23750961C>T dbSNP chr1_000003 0.196 Patients_Q37.5_right 9 46 Admin
0000002389 ./. 1 g.23750961C>T dbSNP chr1_000003 0.069 Patients_Q37 4 58 Admin
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