List of variants in gene PTCH2 reported as benign for basal cell carcinoma, susceptibility to

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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: 16

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HGVS	dbSNP	gnomAD frequency
NM_003738.5(PTCH2):c.2963C>T (p.Thr988Met)	rs11573590	0.02555
NM_003738.5(PTCH2):c.2127C>T (p.Asp709=)	rs11573587	0.01447
NM_003738.5(PTCH2):c.687C>T (p.Ala229=)	rs11573576	0.01288
NM_003738.5(PTCH2):c.2355C>T (p.Tyr785=)	rs11573588	0.01285
NM_003738.5(PTCH2):c.90G>A (p.Leu30=)	rs45573433	0.00945
NM_003738.5(PTCH2):c.1371+8A>G	rs187485698	0.00661
NM_003738.5(PTCH2):c.1080G>T (p.Val360=)	rs11573579	0.00649
NM_003738.5(PTCH2):c.840T>C (p.Ser280=)	rs147627670	0.00534
NM_003738.5(PTCH2):c.2565C>T (p.Leu855=)	rs34245589	0.00406
NM_003738.5(PTCH2):c.2695+8T>C	rs145066065	0.00211
NM_003738.5(PTCH2):c.1425G>A (p.Ala475=)	rs35851686	0.00152
NM_003738.5(PTCH2):c.1569G>A (p.Ala523=)	rs143390610	0.00084
NM_003738.5(PTCH2):c.1596C>T (p.Ala532=)	rs140921885	0.00066
NM_003738.5(PTCH2):c.44C>T (p.Thr15Ile)	rs561781541	0.00003
NM_003738.5(PTCH2):c.1864C>T (p.His622Tyr)	rs11573586
NM_003738.5(PTCH2):c.2427G>C (p.Ser809=)	rs111471526

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