List of variants in gene combination POF1B, ZNF711 reported as benign for X-linked disease

Minimum submission review status:		Collection method:
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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001330574.2(ZNF711):c.*632A>G	rs6653049	0.22070
NM_024921.4(POF1B):c.*1626G>A	rs16980188	0.22046
NM_024921.4(POF1B):c.*1431A>C	rs16980189	0.22033
NM_024921.4(POF1B):c.*1849G>A	rs73513629	0.08686
NM_001330574.2(ZNF711):c.*1411G>A	rs779890560	0.00296
NM_001330574.2(ZNF711):c.*1260G>A	rs73234669	0.00178

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