All genomic variants

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

Effect     

Chr     

AscendingDNA change (genomic) (hg38)     

Reference     

DB-ID     

Frequency     

Allele Count     

Allele Number     

Owner     
0000000277 ./. 1 g.228004696G>A dbSNP chr1_000006 0.664 Control 469 706 Admin
0000000771 ./. 1 g.228004696G>A dbSNP chr1_000006 0.500 Patients_Q37.0 1 2 Admin
0000000920 ./. 1 g.228004696G>A dbSNP chr1_000006 1.000 Patients_Q37.2 4 4 Admin
0000001092 ./. 1 g.228004696G>A dbSNP chr1_000006 1.000 Patients_Q37.3_left 4 4 Admin
0000001270 ./. 1 g.228004696G>A dbSNP chr1_000006 0.167 Patients_Q37.3_right 1 6 Admin
0000001476 ./. 1 g.228004696G>A dbSNP chr1_000006 0.642 Patients_Q37.4 68 106 Admin
0000001720 ./. 1 g.228004696G>A dbSNP chr1_000006 0.750 Patients_Q37.5 3 4 Admin
0000001908 ./. 1 g.228004696G>A dbSNP chr1_000006 0.703 Patients_Q37.5_left 83 118 Admin
0000002161 ./. 1 g.228004696G>A dbSNP chr1_000006 0.674 Patients_Q37.5_right 31 46 Admin
0000002411 ./. 1 g.228004696G>A dbSNP chr1_000006 0.714 Patients_Q37 40 56 Admin
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