List of variants in gene ZNF365 reported as benign

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_014951.3(ZNF365):c.924+34A>G	rs2893897	0.99959
NM_014951.3(ZNF365):c.744-30C>A	rs3852424	0.98590
NM_014951.3(ZNF365):c.743+56G>C	rs1873686	0.96843
NM_014951.3(ZNF365):c.962+210A>G	rs2306970	0.65643
NM_014951.3(ZNF365):c.743+180C>T	rs1873687	0.54931
NM_014951.3(ZNF365):c.1009G>T (p.Ala337Ser)	rs3758490	0.47192
NC_000010.11:g.62666296G>T	rs4746516	0.36843
NM_014951.3(ZNF365):c.743+16_743+17del	rs149800343	0.30229
NM_199450.3(ZNF365):c.925-204C>A	rs11818163	0.20872
NC_000010.11:g.62622902G>A	rs12774545	0.14609
NC_000010.11:g.62656530A>G	rs12776269	0.09765
NM_199450.3(ZNF365):c.*54A>G	rs11819488	0.06086
NC_000010.11:g.62666038C>T	rs111695652	0.01905
NM_199450.3(ZNF365):c.*91A>G	rs78864773	0.01875
NC_000010.11:g.62666162C>A	rs73289245	0.00520
NC_000010.11:g.62670237A>G	rs74156089	0.00439
NC_000010.11:g.62656460C>T	rs76895268	0.00217

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