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     
0000000254 ./. 1 g.23757159T>C dbSNP chr1_000005 0.230 Control 157 684 Admin
0000000905 ./. 1 g.23757159T>C dbSNP chr1_000005 0.250 Patients_Q37.2 1 4 Admin
0000001079 ./. 1 g.23757159T>C dbSNP chr1_000005 0.250 Patients_Q37.3_left 1 4 Admin
0000001453 ./. 1 g.23757159T>C dbSNP chr1_000005 0.186 Patients_Q37.4 19 102 Admin
0000001885 ./. 1 g.23757159T>C dbSNP chr1_000005 0.254 Patients_Q37.5_left 30 118 Admin
0000002138 ./. 1 g.23757159T>C dbSNP chr1_000005 0.283 Patients_Q37.5_right 13 46 Admin
0000002388 ./. 1 g.23757159T>C dbSNP chr1_000005 0.179 Patients_Q37 10 56 Admin
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