List of variants in gene COL18A1 reported as uncertain significance by Athena Diagnostics Inc

Minimum submission review status:		Collection method:
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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001379500.1(COL18A1):c.1882G>A (p.Ala628Thr)	rs181012655	0.00066
NM_001379500.1(COL18A1):c.107-12197G>A	rs200284308	0.00063
NM_001379500.1(COL18A1):c.2623A>G (p.Asn875Asp)	rs371993501	0.00016
NM_001379500.1(COL18A1):c.803C>T (p.Ala268Val)	rs375414087	0.00004
NM_001379500.1(COL18A1):c.1072G>C (p.Gly358Arg)	rs62000458	0.00001
NM_001379500.1(COL18A1):c.1341_1358del (p.Gln451_Pro456del)	rs753322378
NM_001379500.1(COL18A1):c.1343_1351dup (p.Pro448_Pro450dup)	rs775305174
NM_001379500.1(COL18A1):c.1791TGGGCCCCC[1] (p.594PGP[3])	rs764710670
NM_001379500.1(COL18A1):c.738+5G>T	rs1555859077

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