List of variants in gene MSH2 reported by GenomeConnect - Invitae Patient Insights Network

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.128A>G (p.Tyr43Cys)	rs17217723	0.00010
NM_000251.3(MSH2):c.2308A>G (p.Ile770Val)	rs63750684	0.00009
NM_000251.3(MSH2):c.1321A>C (p.Thr441Pro)	rs587779086	0.00006
NM_000251.3(MSH2):c.220A>C (p.Asn74His)	rs150548839	0.00002
NM_000251.3(MSH2):c.2379G>T (p.Gln793His)	rs767520406	0.00002
NM_000251.3(MSH2):c.1175A>T (p.Lys392Met)	rs61756465	0.00001
NM_000251.3(MSH2):c.1927G>A (p.Glu643Lys)	rs374840361	0.00001
NM_000251.3(MSH2):c.242G>A (p.Ser81Asn)	rs1064793491	0.00001
NM_000251.3(MSH2):c.566C>G (p.Ala189Gly)	rs141021599	0.00001
NM_000251.3(MSH2):c.1216C>G (p.Arg406Gly)	rs63751108
NM_000251.3(MSH2):c.655dup (p.Arg219fs)	rs1558461615
NM_000251.3(MSH2):c.998G>A (p.Cys333Tyr)	rs63750828

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