Variants in gene COL18A1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 24

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HGVS	dbSNP	gnomAD frequency
NM_001379500.1(COL18A1):c.2620+29C>T	rs73370840	0.16080
NM_001379500.1(COL18A1):c.2117C>G (p.Pro706Arg)	rs79980197	0.07777
NM_001379500.1(COL18A1):c.2340G>C (p.Gln780His)	rs2230693	0.03222
NM_001379500.1(COL18A1):c.107-12566A>T	rs61735029	0.01258
NM_001379500.1(COL18A1):c.1009G>A (p.Gly337Ser)	rs76547444	0.01152
NM_001379500.1(COL18A1):c.241C>T (p.Arg81Trp)	rs76658745	0.01115
NM_001379500.1(COL18A1):c.2173G>A (p.Val725Met)	rs116111018	0.00795
NM_001379500.1(COL18A1):c.107-12656C>T	rs7277693	0.00639
NM_001379500.1(COL18A1):c.2379+7C>T	rs202100967	0.00379
NM_001379500.1(COL18A1):c.2032-9T>A	rs144913625	0.00375
NM_001379500.1(COL18A1):c.1675-6G>A	rs142726108	0.00263
NM_001379500.1(COL18A1):c.1203T>C (p.Pro401=)	rs375400196	0.00126
NM_001379500.1(COL18A1):c.1254C>T (p.Asp418=)	rs368594049	0.00117
NM_001379500.1(COL18A1):c.693G>A (p.Val231=)	rs149772252	0.00108
NM_001379500.1(COL18A1):c.107-12541A>G	rs200354859	0.00090
NM_001379500.1(COL18A1):c.2478G>A (p.Pro826=)	rs369390092	0.00071
NM_001379500.1(COL18A1):c.107-12121C>T	rs746406313	0.00021
NM_001379500.1(COL18A1):c.1683A>G (p.Ala561=)	rs75222922	0.00016
NM_001379500.1(COL18A1):c.578G>A (p.Arg193Gln)	rs2236453	0.00014
NM_001379500.1(COL18A1):c.2388C>T (p.Tyr796=)	rs139122081	0.00010
NM_001379500.1(COL18A1):c.2032-10G>A	rs368213286	0.00004
NM_001379500.1(COL18A1):c.107-12195G>A	rs62000960
NM_001379500.1(COL18A1):c.1158C>G (p.Pro386=)	rs533684137
NM_001379500.1(COL18A1):c.929-4C>A	rs370679863

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