List of variants in gene combination ATP6V0A2, LOC130009117, 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_012463.3(ATP6V0A2):c.-222C>G	rs71458814	0.36518
NM_012463.4(ATP6V0A2):c.-14C>T	rs1139320	0.36505

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