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

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.245C>T (p.Pro82Leu)	rs1190756871	0.00001
NM_000179.3(MSH6):c.247G>A (p.Ala83Thr)	rs755964436
NM_000179.3(MSH6):c.248C>A (p.Ala83Asp)	rs876661197
NM_000179.3(MSH6):c.248C>G (p.Ala83Gly)	rs876661197
NM_000179.3(MSH6):c.251C>T (p.Ala84Val)	rs878853717
NM_000179.3(MSH6):c.254C>T (p.Pro85Leu)	rs1060502945
NM_000179.3(MSH6):c.259A>C (p.Ser87Arg)	rs1064793939
NM_000179.3(MSH6):c.260+4G>A	rs1389301978

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