ClinVar Miner

List of variants in gene PTCH1 reported as uncertain significance for See cases

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP
GRCh38/hg38 9q22.32(chr9:95516880-95521983)x3

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