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     
0000000346 ./. 9 g.95441917C>T dbSNP chr9_000002 0.454 Control 323 712 Admin
0000000816 ./. 9 g.95441917C>T dbSNP chr9_000002 0.500 Patients_Q37.0 1 2 Admin
0000000968 ./. 9 g.95441917C>T dbSNP chr9_000002 0.750 Patients_Q37.2 3 4 Admin
0000001330 ./. 9 g.95441917C>T dbSNP chr9_000002 0.167 Patients_Q37.3_right 1 6 Admin
0000001545 ./. 9 g.95441917C>T dbSNP chr9_000002 0.443 Patients_Q37.4 47 106 Admin
0000001774 ./. 9 g.95441917C>T dbSNP chr9_000002 0.250 Patients_Q37.5 1 4 Admin
0000001977 ./. 9 g.95441917C>T dbSNP chr9_000002 0.442 Patients_Q37.5_left 53 120 Admin
0000002230 ./. 9 g.95441917C>T dbSNP chr9_000002 0.417 Patients_Q37.5_right 20 48 Admin
0000002479 ./. 9 g.95441917C>T dbSNP chr9_000002 0.328 Patients_Q37 19 58 Admin
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