List of variants in gene COL4A4 reported as likely benign by Counsyl

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000092.5(COL4A4):c.4091-336C>T	rs925971110	0.00003
NM_000092.5(COL4A4):c.4091-356_4091-355dup	rs1553620826	0.00003
NM_000092.5(COL4A4):c.4091-330T>C	rs774439386	0.00002
NM_000092.5(COL4A4):c.3978A>G (p.Pro1326=)	rs780675797	0.00001
NM_000092.5(COL4A4):c.3984A>T (p.Gly1328=)	rs750748339	0.00001
NM_000092.5(COL4A4):c.4038T>C (p.Gly1346=)	rs565940301	0.00001
NM_000092.5(COL4A4):c.4053A>G (p.Pro1351=)	rs1553624041	0.00001
NM_000092.5(COL4A4):c.4081+7T>C	rs779775976	0.00001
NM_000092.5(COL4A4):c.4081+15T>C	rs1356475870
NM_000092.5(COL4A4):c.4081+22A>C	rs1553623967
NM_000092.5(COL4A4):c.4081+22A>G	rs1553623967
NM_000092.5(COL4A4):c.4091-323A>G	rs774221440
NM_000092.5(COL4A4):c.4091-346A>G	rs753906137
NM_000092.5(COL4A4):c.4091-348T>C	rs1553620812
NM_000092.5(COL4A4):c.4091-349G>A	rs1434118080

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