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     
0000000303 ./. 4 g.123394883A>G dbSNP chr4_000001 0.833 Control 578 694 Admin
0000000787 ./. 4 g.123394883A>G dbSNP chr4_000001 0.500 Patients_Q37.0 1 2 Admin
0000000937 ./. 4 g.123394883A>G dbSNP chr4_000001 0.500 Patients_Q37.2 2 4 Admin
0000001112 ./. 4 g.123394883A>G dbSNP chr4_000001 0.750 Patients_Q37.3_left 3 4 Admin
0000001292 ./. 4 g.123394883A>G dbSNP chr4_000001 0.667 Patients_Q37.3_right 4 6 Admin
0000001502 ./. 4 g.123394883A>G dbSNP chr4_000001 0.810 Patients_Q37.4 81 100 Admin
0000001739 ./. 4 g.123394883A>G dbSNP chr4_000001 1.000 Patients_Q37.5 2 2 Admin
0000001934 ./. 4 g.123394883A>G dbSNP chr4_000001 0.754 Patients_Q37.5_left 89 118 Admin
0000002187 ./. 4 g.123394883A>G dbSNP chr4_000001 0.795 Patients_Q37.5_right 35 44 Admin
0000002436 ./. 4 g.123394883A>G dbSNP chr4_000001 0.741 Patients_Q37 43 58 Admin
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