List of variants in gene combination PCDH12, RNF14 reported as benign by Genome-Nilou Lab

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_016580.4(PCDH12):c.192T>C (p.Ala64=)	rs164077	0.73075
NM_016580.4(PCDH12):c.2176T>C (p.Leu726=)	rs164073	0.67454
NM_016580.4(PCDH12):c.1153C>A (p.His385Asn)	rs164075	0.64019
NM_016580.4(PCDH12):c.2133C>T (p.Ala711=)	rs164074	0.49888
NM_016580.4(PCDH12):c.291G>A (p.Leu97=)	rs164076	0.47857
NM_016580.4(PCDH12):c.2496G>A (p.Gln832=)	rs2434322	0.09860

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