List of variants in gene combination ATP6V0A2, TCTN2 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)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_024809.5(TCTN2):c.*67C>T	rs112214860	0.01216
NM_024809.5(TCTN2):c.*45G>A	rs142969969	0.01053
NM_024809.5(TCTN2):c.2041T>C (p.Leu681=)	rs112158562	0.01028

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