List of variants in gene ADAM9 reported as pathogenic for not provided

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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)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_003816.3(ADAM9):c.490C>T (p.Arg164Ter)	rs137853041	0.00001
NC_000008.10:g.(?_38911980)_(38928942_?)del
NC_000008.10:g.(?_38913076)_(38928942_?)del
NC_000008.11:g.39018852GA[1]
NM_003816.3(ADAM9):c.1284_1285del (p.Cys428_Asp429delinsTer)
NM_003816.3(ADAM9):c.1420C>T (p.Arg474Ter)	rs2129438784
NM_003816.3(ADAM9):c.1802G>A (p.Trp601Ter)
NM_003816.3(ADAM9):c.196-1G>A	rs1057518208
NM_003816.3(ADAM9):c.1968T>A (p.Cys656Ter)	rs1422732315
NM_003816.3(ADAM9):c.399T>A (p.Cys133Ter)
NM_003816.3(ADAM9):c.543_546dup (p.Glu183fs)	rs2129433185
NM_003816.3(ADAM9):c.735C>A (p.Tyr245Ter)

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