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     
0000000276 ./. 1 g.228005052T>A dbSNP chr1_000007 0.560 Control 391 698 Admin
0000000919 ./. 1 g.228005052T>A dbSNP chr1_000007 1.000 Patients_Q37.2 4 4 Admin
0000001091 ./. 1 g.228005052T>A dbSNP chr1_000007 1.000 Patients_Q37.3_left 4 4 Admin
0000001475 ./. 1 g.228005052T>A dbSNP chr1_000007 0.500 Patients_Q37.4 50 100 Admin
0000001719 ./. 1 g.228005052T>A dbSNP chr1_000007 1.000 Patients_Q37.5 2 2 Admin
0000001907 ./. 1 g.228005052T>A dbSNP chr1_000007 0.509 Patients_Q37.5_left 59 116 Admin
0000002160 ./. 1 g.228005052T>A dbSNP chr1_000007 0.457 Patients_Q37.5_right 21 46 Admin
0000002410 ./. 1 g.228005052T>A dbSNP chr1_000007 0.625 Patients_Q37 35 56 Admin
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