List of variants in gene MSH2 reported as benign by Eurofins NTD LLC (GA)

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.211+9C>G	rs2303426	0.55454
NM_000251.3(MSH2):c.1661+12G>A	rs3732183	0.40290
NM_000251.3(MSH2):c.1511-9A>T	rs12998837	0.09123
NM_000251.3(MSH2):c.367-168C>T	rs17217758	0.08993
NM_000251.3(MSH2):c.2006-6T>C	rs2303428	0.08349
NM_000251.3(MSH2):c.380A>G (p.Asn127Ser)	rs17217772	0.02317
NM_000251.3(MSH2):c.1077-10T>C	rs17224360	0.01428
NM_000251.3(MSH2):c.1666T>C (p.Leu556=)	rs61756466	0.00471
NM_000251.3(MSH2):c.339G>A (p.Lys113=)	rs35898375	0.00313
NM_000251.3(MSH2):c.1277-8T>C	rs145400590	0.00159
NM_000251.3(MSH2):c.1168C>T (p.Leu390Phe)	rs17224367	0.00039

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