List of variants in gene MSH2 reported by Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.965G>A (p.Gly322Asp)	rs4987188	0.01714
NM_000251.3(MSH2):c.1748A>G (p.Asn583Ser)	rs201118107	0.00014
NM_000251.3(MSH2):c.212-3A>T	rs879255341	0.00001
NM_000251.3(MSH2):c.2197G>A (p.Ala733Thr)	rs772662439	0.00001
NM_000251.3(MSH2):c.942+17_942+29del	rs11309117
NM_000251.3(MSH2):c.942+25_942+29del	rs11309117

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