All genomic variants

9 entries on 1 page. Showing entries 1 - 9.
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Variant ID     

Effect     

Chr     

AscendingDNA change (genomic) (hg38)     

Reference     

DB-ID     

Frequency     

Allele Count     

Allele Number     

Owner     
0000000323 ./. 6 g.83526030G>T dbSNP chr6_000001 0.480 Control 340 708 Admin
0000000806 ./. 6 g.83526030G>T dbSNP chr6_000001 1.000 Patients_Q37.0 2 2 Admin
0000001127 ./. 6 g.83526030G>T dbSNP chr6_000001 0.250 Patients_Q37.3_left 1 4 Admin
0000001310 ./. 6 g.83526030G>T dbSNP chr6_000001 0.333 Patients_Q37.3_right 2 6 Admin
0000001522 ./. 6 g.83526030G>T dbSNP chr6_000001 0.566 Patients_Q37.4 60 106 Admin
0000001758 ./. 6 g.83526030G>T dbSNP chr6_000001 0.500 Patients_Q37.5 2 4 Admin
0000001954 ./. 6 g.83526030G>T dbSNP chr6_000001 0.517 Patients_Q37.5_left 62 120 Admin
0000002207 ./. 6 g.83526030G>T dbSNP chr6_000001 0.354 Patients_Q37.5_right 17 48 Admin
0000002456 ./. 6 g.83526030G>T dbSNP chr6_000001 0.569 Patients_Q37 33 58 Admin
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