List of variants in gene combination FBXO11, MSH6 reported as likely benign 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.4002-25T>C	rs199500983	0.00004
NM_000179.3(MSH6):c.3647-6T>C	rs182871847
NM_000179.3(MSH6):c.4002-8A>T	rs778957100
NM_000179.3(MSH6):c.4068_4071dup (p.Lys1358delinsAspTer)	rs55740729

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