List of variants in gene combination PCDH12, RNF14 reported by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_016580.4(PCDH12):c.152A>G (p.Gln51Arg)	rs138473035	0.00025
NM_016580.4(PCDH12):c.1060G>A (p.Val354Ile)	rs763363704	0.00004
NM_016580.4(PCDH12):c.2374G>A (p.Gly792Arg)	rs138811155	0.00003
NM_016580.4(PCDH12):c.922C>T (p.Arg308Ter)	rs370283860	0.00003
NM_016580.4(PCDH12):c.1493G>A (p.Arg498His)	rs374457419	0.00002

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