List of variants in gene combination PCDH12, RNF14 reported as benign by PreventionGenetics, part of Exact Sciences

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_016580.4(PCDH12):c.2496G>A (p.Gln832=)	rs2434322	0.09860
NM_016580.4(PCDH12):c.240C>G (p.Asp80Glu)	rs138689340	0.01052
NM_016580.4(PCDH12):c.2635C>G (p.Pro879Ala)	rs61737138	0.00503
NM_016580.4(PCDH12):c.1735G>A (p.Val579Met)	rs114449118	0.00344
NM_016580.4(PCDH12):c.2051C>G (p.Pro684Arg)	rs10040926

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