List of variants in gene combination LRRFIP2, MLH1 reported as pathogenic for colorectal cancer

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: 3

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 3p22.2(chr3:37089011-37116538)
NC_000003.11:g.(?_37092052)_(37100470_?)del
NC_000003.11:g.37089454_37101079del

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