ClinVar Miner

List of variants in gene PTCH1 reported as likely benign for Basal cell carcinoma, susceptibility to, 1; Basal cell nevus syndrome 1

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000264.5(PTCH1):c.4324C>T (p.Arg1442Trp)	rs143464326	0.00060
NM_000264.5(PTCH1):c.1602+15_1602+17del	rs528001004

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