List of variants in gene COL4A5 reported as benign by PreventionGenetics, part of Exact Sciences

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_033380.3(COL4A5):c.3513A>G (p.Gln1171=)	rs2273051	0.14310
NM_033380.3(COL4A5):c.2349G>A (p.Pro783=)	rs3747408	0.11046
NM_033380.3(COL4A5):c.1331T>G (p.Ile444Ser)	rs2272946	0.11020
NM_033380.3(COL4A5):c.2055T>C (p.Leu685=)	rs7884085	0.10905
NM_033380.3(COL4A5):c.1095G>C (p.Gly365=)	rs2272945	0.10302
NM_033380.3(COL4A5):c.4293C>T (p.Asp1431=)	rs61746140	0.10149
NM_033380.3(COL4A5):c.2768-11A>G	rs1006269	0.09324
NM_033380.3(COL4A5):c.3519T>G (p.Gly1173=)	rs61735627	0.03239
NM_033380.3(COL4A5):c.1992G>T (p.Lys664Asn)	rs34077552	0.00745
NM_033380.3(COL4A5):c.4223C>G (p.Thr1408Ser)	rs151278542	0.00294
NM_033380.3(COL4A5):c.3148C>T (p.Pro1050Ser)	rs143945573	0.00155
NM_033380.3(COL4A5):c.2858G>T (p.Gly953Val)	rs78972735	0.00119
NM_033380.3(COL4A5):c.580A>G (p.Ile194Val)	rs145970300	0.00099

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