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     
0000000291 ./. 2 g.202238678G>A dbSNP chr2_000001 0.423 Control 302 714 Admin
0000001102 ./. 2 g.202238678G>A dbSNP chr2_000001 0.500 Patients_Q37.3_left 2 4 Admin
0000001281 ./. 2 g.202238678G>A dbSNP chr2_000001 0.167 Patients_Q37.3_right 1 6 Admin
0000001490 ./. 2 g.202238678G>A dbSNP chr2_000001 0.349 Patients_Q37.4 37 106 Admin
0000001729 ./. 2 g.202238678G>A dbSNP chr2_000001 0.250 Patients_Q37.5 1 4 Admin
0000001922 ./. 2 g.202238678G>A dbSNP chr2_000001 0.325 Patients_Q37.5_left 39 120 Admin
0000002175 ./. 2 g.202238678G>A dbSNP chr2_000001 0.354 Patients_Q37.5_right 17 48 Admin
0000002424 ./. 2 g.202238678G>A dbSNP chr2_000001 0.448 Patients_Q37 26 58 Admin
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