List of variants in gene combination DLC1, LOC126860305 reported as likely benign for Colorectal cancer

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_182643.3(DLC1):c.3856-6G>A	rs200102232	0.00179
NM_182643.3(DLC1):c.3968A>T (p.His1323Leu)
NM_182643.3(DLC1):c.4067A>G (p.Tyr1356Cys)

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