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     
0000000371 ./. 11 g.76185603C>T dbSNP chr11_000002 0.228 Control 162 710 Admin
0000000829 ./. 11 g.76185603C>T dbSNP chr11_000002 0.500 Patients_Q37.0 1 2 Admin
0000000987 ./. 11 g.76185603C>T dbSNP chr11_000002 0.500 Patients_Q37.2 2 4 Admin
0000001160 ./. 11 g.76185603C>T dbSNP chr11_000002 0.750 Patients_Q37.3_left 3 4 Admin
0000001352 ./. 11 g.76185603C>T dbSNP chr11_000002 0.333 Patients_Q37.3_right 2 6 Admin
0000001570 ./. 11 g.76185603C>T dbSNP chr11_000002 0.330 Patients_Q37.4 35 106 Admin
0000001790 ./. 11 g.76185603C>T dbSNP chr11_000002 0.250 Patients_Q37.5 1 4 Admin
0000002002 ./. 11 g.76185603C>T dbSNP chr11_000002 0.271 Patients_Q37.5_left 32 118 Admin
0000002255 ./. 11 g.76185603C>T dbSNP chr11_000002 0.188 Patients_Q37.5_right 9 48 Admin
0000002504 ./. 11 g.76185603C>T dbSNP chr11_000002 0.241 Patients_Q37 14 58 Admin
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