List of variants in gene MSH2 studied for Colorectal cancer, non-polyposis

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.815C>T (p.Ala272Val)	rs34136999	0.00046
NM_000251.3(MSH2):c.435T>G (p.Ile145Met)	rs63750124	0.00031
NM_000251.3(MSH2):c.1787A>G (p.Asn596Ser)	rs41295288	0.00022
NM_000251.3(MSH2):c.1748A>G (p.Asn583Ser)	rs201118107	0.00014
NM_000251.3(MSH2):c.913G>A (p.Ala305Thr)	rs63751454	0.00008
NM_000251.3(MSH2):c.499G>C (p.Asp167His)	rs63750255	0.00006
NM_000251.3(MSH2):c.968C>G (p.Ser323Cys)	rs63750732	0.00003
NM_000251.3(MSH2):c.1418C>T (p.Ser473Leu)	rs63751403	0.00001
NM_000251.3(MSH2):c.2437A>G (p.Met813Val)	rs63749841	0.00001
NM_000251.3(MSH2):c.2768T>A (p.Val923Glu)	rs146421227	0.00001

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