List of variants in gene COL4A5 reported as uncertain significance by Gharavi Laboratory, Columbia University

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_033380.3(COL4A5):c.4567C>A (p.Pro1523Thr)	rs201220208	0.00014
NM_033380.3(COL4A5):c.4246C>T (p.Arg1416Cys)	rs104886270	0.00008
NM_033380.3(COL4A5):c.4898C>T (p.Ala1633Val)	rs982188184	0.00006
NM_033380.3(COL4A5):c.146A>G (p.Glu49Gly)	rs1569486475
NM_033380.3(COL4A5):c.4155_4157del (p.Ile1386del)	rs1569507545
NM_033380.3(COL4A5):c.4282C>T (p.Arg1428Cys)	rs144282156
NM_033380.3(COL4A5):c.4960T>C (p.Trp1654Arg)	rs1569509354
NM_033380.3(COL4A5):c.572_583del (p.Pro191_Gly195delinsArg)	rs1569489843

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