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
0000209087 ./. 1 g.139247_139248insAGCTGGGTGTGTAGA - chr1_000018 - - - - Admin
0000209095 ./. 1 g.494547C>T dbSNP chr1_000018 0.033 5 150 1283 Admin
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