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     
0000000372 ./. 13 g.80335808C>T dbSNP chr13_000002 0.066 Control 47 710 Admin
0000000830 ./. 13 g.80335808C>T dbSNP chr13_000002 0.500 Patients_Q37.0 1 2 Admin
0000000988 ./. 13 g.80335808C>T dbSNP chr13_000002 0.250 Patients_Q37.2 1 4 Admin
0000001353 ./. 13 g.80335808C>T dbSNP chr13_000002 0.167 Patients_Q37.3_right 1 6 Admin
0000001571 ./. 13 g.80335808C>T dbSNP chr13_000002 0.098 Patients_Q37.4 10 102 Admin
0000002003 ./. 13 g.80335808C>T dbSNP chr13_000002 0.079 Patients_Q37.5_left 9 114 Admin
0000002256 ./. 13 g.80335808C>T dbSNP chr13_000002 0.087 Patients_Q37.5_right 4 46 Admin
0000002505 ./. 13 g.80335808C>T dbSNP chr13_000002 0.017 Patients_Q37 1 58 Admin
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