List of variants in gene PTCH1 reported as likely benign for basal cell carcinoma, susceptibility to, 1

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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_000264.5(PTCH1):c.318C>T (p.Leu106=)	rs1805153	0.01567
NM_001083603.1(PTCH1):c.131A>G (p.Glu44Gly)	rs202111971	0.00732
NM_000264.5(PTCH1):c.1119C>T (p.Tyr373=)	rs2066831	0.00677
NM_000264.5(PTCH1):c.1074T>C (p.His358=)	rs2066832	0.00674
NM_000264.5(PTCH1):c.4048C>T (p.Arg1350Trp)	rs140417636	0.00086
NM_000264.5(PTCH1):c.4001G>A (p.Ser1334Asn)	rs200620662	0.00016
NM_000264.5(PTCH1):c.4013G>A (p.Arg1338His)	rs771238114	0.00005
NM_000264.5(PTCH1):c.584+10G>A	rs765713791	0.00004

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