List of variants in gene combination B9D1, LOC130060455 reported as likely benign for Meckel syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_015681.6(B9D1):c.33C>T (p.Leu11=)	rs751480715	0.00004
NM_015681.6(B9D1):c.30A>C (p.Leu10=)	rs781395275
NM_015681.6(B9D1):c.63+11G>A	rs2152278747
NM_015681.6(B9D1):c.63+16C>T
NM_015681.6(B9D1):c.63+20G>A	rs765907063
NM_015681.6(B9D1):c.63+20_63+43del	rs2152278609
NM_015681.6(B9D1):c.9C>G (p.Thr3=)	rs749611797

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