List of variants in gene PTCH2 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_003738.5(PTCH2):c.90G>A (p.Leu30=)	rs45573433	0.00945
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.1083+3C>T	rs557532187	0.00066
NM_003738.5(PTCH2):c.44C>T (p.Thr15Ile)	rs561781541	0.00003
NM_003738.5(PTCH2):c.1760G>A (p.Gly587Glu)	rs772982125	0.00001
NM_003738.5(PTCH2):c.1864C>T (p.His622Tyr)	rs11573586
NM_003738.5(PTCH2):c.2427G>C (p.Ser809=)	rs111471526

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