List of variants in gene combination COL5A1, LOC101448202 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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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_000093.5(COL5A1):c.5407G>A (p.Asp1803Asn)	rs61729495	0.00394
NM_000093.5(COL5A1):c.4676A>C (p.His1559Pro)	rs768691969	0.00021
NM_000093.5(COL5A1):c.4643C>T (p.Ser1548Leu)	rs147398633	0.00011
NM_000093.5(COL5A1):c.5097C>G (p.Asn1699Lys)	rs138396959	0.00009
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.4905C>T (p.Pro1635=)	rs760426595	0.00003
NM_000093.5(COL5A1):c.5294G>A (p.Arg1765His)	rs150608071	0.00002
NM_000093.5(COL5A1):c.5437G>A (p.Val1813Met)	rs755914340	0.00002
NM_000093.5(COL5A1):c.4503C>T (p.Gly1501=)
NM_000093.5(COL5A1):c.4555-17T>A
NM_000093.5(COL5A1):c.4893G>A (p.Thr1631=)
NM_000093.5(COL5A1):c.5136+102C>G
NM_000093.5(COL5A1):c.5350G>A (p.Ala1784Thr)	rs143859495
NM_000093.5(COL5A1):c.5371-14T>C

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