List of variants in gene ATP6V0A2 reported as benign for not specified

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_012463.4(ATP6V0A2):c.1515T>C (p.Asn505=)	rs7135542	0.71178
NM_012463.4(ATP6V0A2):c.426T>C (p.Asn142=)	rs1139789	0.66312
NM_012463.4(ATP6V0A2):c.471T>C (p.Ser157=)	rs1399961	0.66054
NM_012463.4(ATP6V0A2):c.432+14C>T	rs11837144	0.65907
NM_012463.4(ATP6V0A2):c.2438C>T (p.Ala813Val)	rs17883456	0.02527
NM_012463.4(ATP6V0A2):c.1121A>G (p.Lys374Arg)	rs79134187	0.02323
NM_012463.4(ATP6V0A2):c.1016G>A (p.Arg339His)	rs74922060	0.01800
NM_012463.4(ATP6V0A2):c.1039-14T>C	rs115569365	0.01308
NM_012463.4(ATP6V0A2):c.2549A>G (p.Asn850Ser)	rs75279884	0.01166
NM_012463.4(ATP6V0A2):c.1606-12G>A	rs112415338	0.01148
NM_012463.4(ATP6V0A2):c.777G>A (p.Arg259=)	rs73420336	0.00931
NM_012463.4(ATP6V0A2):c.2054G>A (p.Arg685Gln)	rs7969410	0.00727
NM_012463.4(ATP6V0A2):c.1258G>T (p.Val420Leu)	rs138716143	0.00258
NM_012463.4(ATP6V0A2):c.2238C>T (p.Cys746=)	rs138886791	0.00150
NM_012463.4(ATP6V0A2):c.1590C>T (p.Pro530=)	rs80355657	0.00078
NM_012463.4(ATP6V0A2):c.2466-4_2466-3del	rs370511382
NM_012463.4(ATP6V0A2):c.732-23T>C	rs2271660

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