All genomic variants

7 entries on 1 page. Showing entries 1 - 7.
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Variant ID     

Effect     

Chr     

AscendingDNA change (genomic) (hg38)     

Reference     

DB-ID     

Frequency     

Allele Count     

Allele Number     

Owner     
0000000307 ./. 5 g.138083805G>T dbSNP chr5_000001 0.121 Control 86 712 Admin
0000000791 ./. 5 g.138083805G>T dbSNP chr5_000001 0.500 Patients_Q37.0 1 2 Admin
0000001295 ./. 5 g.138083805G>T dbSNP chr5_000001 0.333 Patients_Q37.3_right 2 6 Admin
0000001506 ./. 5 g.138083805G>T dbSNP chr5_000001 0.176 Patients_Q37.4 18 102 Admin
0000001938 ./. 5 g.138083805G>T dbSNP chr5_000001 0.136 Patients_Q37.5_left 16 118 Admin
0000002191 ./. 5 g.138083805G>T dbSNP chr5_000001 0.208 Patients_Q37.5_right 10 48 Admin
0000002440 ./. 5 g.138083805G>T dbSNP chr5_000001 0.155 Patients_Q37 9 58 Admin
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