List of variants in gene combination COL18A1, SLC19A1 reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001379500.1(COL18A1):c.3823G>T (p.Val1275Leu)	rs61736805	0.01313
NM_001379500.1(COL18A1):c.3352G>A (p.Ala1118Thr)	rs113268527	0.00717
NM_001379500.1(COL18A1):c.3673G>A (p.Val1225Met)	rs77326997	0.00707
NM_001379500.1(COL18A1):c.2684-14TC[2]	rs148455528
NM_001379500.1(COL18A1):c.2702TTC[1] (p.Leu902del)	rs371849586

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