List of variants in gene combination LOC129933707, MSH6 reported as uncertain significance for Lynch syndrome 5

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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_000179.3(MSH6):c.249T>G (p.Ala83=)	rs876658308	0.00001
NM_000179.3(MSH6):c.253C>T (p.Pro85Ser)	rs779664343
NM_000179.3(MSH6):c.254CCA[1] (p.Thr86del)	rs1553408448

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