List of variants in gene B9D1 reported as likely pathogenic 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)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_015681.6(B9D1):c.341+2T>C	rs143149764	0.00009
NM_015681.6(B9D1):c.341G>A (p.Arg114Gln)	rs778260923	0.00001
NM_015681.6(B9D1):c.342-1G>T
NM_015681.6(B9D1):c.529G>C (p.Asp177His)	rs1309922077

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