List of variants reported as likely benign by Reproductive Health Research and Development, BGI Genomics

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001171.6(ABCC6):c.346-6G>A	rs55778939	0.03265
NM_001171.6(ABCC6):c.4254G>A (p.Arg1418=)	rs58668703	0.00784
NM_001171.6(ABCC6):c.3883-24G>A	rs59513011	0.00475
NM_016097.5(IER3IP1):c.*58T>C	rs150586939	0.00406
NM_001171.6(ABCC6):c.600+23C>T	rs72664290	0.00101
NM_001173990.3(TMEM216):c.216T>C (p.Ile72=)	rs541666319
NM_199461.4(NANOS1):c.231CTC[3] (p.Ser83del)	rs587777031

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