ClinVar Miner

List of variants in gene B9D1 reported as likely benign for Meckel syndrome, type 9

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Minimum conflict level: Report conflict between different conditions
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: 2

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HGVS	dbSNP	gnomAD frequency
NM_015681.6(B9D1):c.580T>C (p.Leu194=)	rs7212549	0.01478
NM_015681.6(B9D1):c.181C>T (p.Arg61Trp)	rs73980038	0.01073

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