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     
0000000327 ./. 6 g.10395339A>G dbSNP chr6_000003 0.440 Control 314 714 Admin
0000000954 ./. 6 g.10395339A>G dbSNP chr6_000003 0.750 Patients_Q37.2 3 4 Admin
0000001130 ./. 6 g.10395339A>G dbSNP chr6_000003 0.750 Patients_Q37.3_left 3 4 Admin
0000001314 ./. 6 g.10395339A>G dbSNP chr6_000003 0.667 Patients_Q37.3_right 4 6 Admin
0000001526 ./. 6 g.10395339A>G dbSNP chr6_000003 0.660 Patients_Q37.4 70 106 Admin
0000001762 ./. 6 g.10395339A>G dbSNP chr6_000003 0.500 Patients_Q37.5 2 4 Admin
0000001958 ./. 6 g.10395339A>G dbSNP chr6_000003 0.551 Patients_Q37.5_left 65 118 Admin
0000002211 ./. 6 g.10395339A>G dbSNP chr6_000003 0.500 Patients_Q37.5_right 24 48 Admin
0000002460 ./. 6 g.10395339A>G dbSNP chr6_000003 0.466 Patients_Q37 27 58 Admin
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