List of variants in gene combination COL5A1, LOC101448202 reported as uncertain significance for not specified

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000093.5(COL5A1):c.4909C>T (p.Arg1637Cys)	rs753433375	0.00003
NM_000093.5(COL5A1):c.5371-8T>C	rs1352923765	0.00002
NM_000093.5(COL5A1):c.4765G>A (p.Ala1589Thr)	rs377138881	0.00001
NM_000093.5(COL5A1):c.4934G>A (p.Cys1645Tyr)	rs863223461	0.00001
NM_000093.5(COL5A1):c.*6G>A
NM_000093.5(COL5A1):c.4954+4A>G	rs1564487377
NM_000093.5(COL5A1):c.4994A>T (p.Asp1665Val)

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