Variants in gene combination COL5A1, LOC101448202 with conflicting interpretations reported as "uncertain significance and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_000093.5(COL5A1):c.4906G>A (p.Ala1636Thr)	rs113452150	0.00092
NM_000093.5(COL5A1):c.4658C>T (p.Pro1553Leu)	rs530570306	0.00007
NM_000093.5(COL5A1):c.5293C>T (p.Arg1765Cys)	rs199703883	0.00005
NM_000093.5(COL5A1):c.4794C>T (p.Gly1598=)	rs863223481	0.00002
NM_000093.5(COL5A1):c.5371-8T>C	rs1352923765	0.00002
NM_000093.5(COL5A1):c.5437G>A (p.Val1813Met)	rs755914340	0.00002
NM_000093.5(COL5A1):c.4831A>C (p.Ile1611Leu)	rs754447923	0.00001
NM_000093.5(COL5A1):c.5206G>A (p.Ala1736Thr)	rs753339980	0.00001
NM_000093.5(COL5A1):c.5350G>A (p.Ala1784Thr)	rs143859495

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