List of variants in gene PTCH2 reported as likely benign for Basal cell carcinoma, susceptibility to, 1; Gorlin syndrome; Medulloblastoma

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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_003738.5(PTCH2):c.3363A>G (p.Ile1121Met)	rs11573598	0.00155
NM_003738.5(PTCH2):c.1994G>A (p.Arg665His)	rs138588008	0.00103
NM_003738.5(PTCH2):c.1780G>A (p.Ala594Thr)	rs147669300	0.00037
NM_003738.5(PTCH2):c.2661C>T (p.His887=)	rs149815763	0.00016

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