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
0000209086 ./. 1 g.139233C>A dbSNP chr1_000017 0.297 63 212 3702 Admin
0000209094 ./. 1 g.494542G>A dbSNP chr1_000017 0.027 4 150 0 Admin
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