List of variants in gene combination B9D1, LOC130060455 reported as 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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_015681.6(B9D1):c.63+23G>A	rs10445411	0.56182
NM_015681.6(B9D1):c.63+19dup	rs2152278724

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