List of variants in gene PTCH1 reported as pathogenic by Juno Genomics, Hangzhou Juno Genomics, Inc

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000264.5(PTCH1):c.1198C>T (p.Gln400Ter)	rs1588605348
NM_000264.5(PTCH1):c.3321_3330del (p.Ile1108fs)
NM_000264.5(PTCH1):c.563dup (p.His189fs)

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