List of variants in gene combination POF1B, ZNF711 reported as likely benign for Non-syndromic X-linked intellectual disability

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_024921.4(POF1B):c.*1173C>A	rs7062790	0.01314
NM_024921.4(POF1B):c.*1808A>G	rs56307558	0.00517
NM_001330574.2(ZNF711):c.*1411G>A	rs779890560	0.00296
NM_001330574.2(ZNF711):c.*1260G>A	rs73234669	0.00178

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