List of variants in gene combination LOC100507346, PTCH1 reported as benign for not specified

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000264.5(PTCH1):c.2560+9G>C	rs2066829	0.44128
NM_000264.5(PTCH1):c.2250+25T>C	rs16909898	0.10561
NM_000264.5(PTCH1):c.2199A>G (p.Ser733=)	rs2227970	0.01091
NM_000264.5(PTCH1):c.1854C>T (p.Cys618=)	rs62637628	0.00887
NM_000264.5(PTCH1):c.2183C>T (p.Thr728Met)	rs115556836	0.00678
NM_000264.5(PTCH1):c.2173C>T (p.Pro725Ser)	rs149258400	0.00098
NM_000264.5(PTCH1):c.2304C>T (p.Thr768=)	rs1805156	0.00086
NM_000264.5(PTCH1):c.1847+14C>T	rs202007968	0.00053
NM_000264.5(PTCH1):c.2560+8G>A	rs201541845	0.00049
NM_000264.5(PTCH1):c.2479A>G (p.Ser827Gly)	rs199476092	0.00036
NM_000264.5(PTCH1):c.2222C>T (p.Ala741Val)	rs2227971	0.00020
NM_000264.5(PTCH1):c.1962G>T (p.Thr654=)	rs201544613

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