All genomic variants

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Variant ID

Effect

Chr

DNA change (genomic) (hg38)

Reference

DB-ID

Frequency

Allele Count

Allele Number

Depth

Owner
0000209089 ./. 1 g.139393G>T dbSNP chr1_000020 0.028 6 212 2796 Admin
0000209098 ./. 1 g.494623_494655delins. - chr1_000020 0.006849 1 146 537 Admin
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