List of variants in gene combination COQ6, ENTPD5 reported as benign for familial nephrotic 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_182476.3(COQ6):c.1210+13A>G	rs7141392	0.84418
NM_182476.3(COQ6):c.1216G>A (p.Val406Met)	rs8500	0.39628
NM_182476.3(COQ6):c.570T>C (p.His190=)	rs3180946	0.30516
NM_182476.3(COQ6):c.1184C>T (p.Thr395Met)	rs34746680	0.00726

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