List of variants reported as uncertain significance for B-cell immunodeficiency, distal limb anomalies, and urogenital malformations by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001330700.2(TOP2B):c.1868T>C (p.Ile623Thr)	rs776496462	0.00004
NM_000381.4(MID1):c.601G>A (p.Val201Ile)
NM_001330700.2(TOP2B):c.1303del (p.Trp435fs)
NM_001330700.2(TOP2B):c.4151A>C (p.Asp1384Ala)

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