List of variants in gene combination AIMP2, PMS2 reported as benign 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
NM_000535.5(PMS2):c.-323G>T	rs1062372	0.23877
NM_000535.5(PMS2):c.-2559T>A	rs78453798	0.04887
NM_000535.5(PMS2):c.-2146C>A	rs77199218	0.04878

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