List of variants in gene combination PCDH12, RNF14 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_016580.4(PCDH12):c.850A>G (p.Ser284Gly)	rs78397925	0.00394
NM_016580.4(PCDH12):c.782C>T (p.Thr261Met)	rs151002555	0.00375
NM_016580.4(PCDH12):c.1735G>A (p.Val579Met)	rs114449118	0.00357
NM_016580.4(PCDH12):c.1236G>A (p.Leu412=)
NM_016580.4(PCDH12):c.1734C>G (p.Ser578=)
NM_016580.4(PCDH12):c.579T>C (p.His193=)

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