ClinVar Miner

List of variants in gene combination COL5A1, LOC101448202 reported as likely benign by Center for Human Genetics, Inc, Center for Human Genetics, Inc

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000093.5(COL5A1):c.5137-12C>T	rs191758714	0.00488
NM_000093.5(COL5A1):c.4515C>T (p.Leu1505=)	rs764114280

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