ClinVar Miner

List of variants in gene PTCH1 reported as benign by Mendelics

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.4219G>A (p.Gly1407Ser)	rs56161606	0.00009
NM_000264.5(PTCH1):c.1016A>G (p.Glu339Gly)	rs777696239

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