List of variants in gene combination ARHGAP11A-SCG5, GREM1, LOC125078054, SCG5 reported as uncertain significance for Familial 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: 4

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HGVS	dbSNP	gnomAD frequency
NC_000015.9:g.(?_32964740)_(33004759_?)dup
NC_000015.9:g.(?_32964740)_(33023456_?)dup
NC_000015.9:g.(?_32976738)_(33023456_?)dup
NC_000015.9:g.(?_32988695)_(33004759_?)dup

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