List of variants reported as uncertain significance for Lynch syndrome 5 by MGZ Medical Genetics Center

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.3961A>G (p.Arg1321Gly)	rs41295278	0.00019
NM_000179.3(MSH6):c.3245C>T (p.Pro1082Leu)	rs191109849	0.00010
NM_000179.3(MSH6):c.2384T>C (p.Ile795Thr)	rs202127474	0.00007
NM_000179.3(MSH6):c.3425C>T (p.Thr1142Met)	rs267608089	0.00005
NM_000179.3(MSH6):c.1103A>G (p.Glu368Gly)	rs1572721697
NM_000179.3(MSH6):c.2075A>G (p.Lys692Arg)	rs975991506
NM_000179.3(MSH6):c.3289C>T (p.Pro1097Ser)
NM_000179.3(MSH6):c.34C>A (p.Pro12Thr)	rs587782084

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