C1333991[trait identifier] AND "HudsonAlpha Institute for Biotechnolog - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 90151	NM_000249.4(MLH1):c.306G>T (p.Glu102Asp)	MLH1 (E102D)	Single nucleotide variant (missense variant +2 more)	Lynch syndrome	GUncertain significance
Select item 90453	NM_000249.4(MLH1):c.955G>T (p.Glu319Ter)	MLH1 (E319* +3 more)	Single nucleotide variant (nonsense +2 more)	Lynch syndrome	GPathogenic
Select item 36540	NM_000249.4(MLH1):c.1381A>T (p.Lys461Ter)	MLH1 (K461* +5 more)	Single nucleotide variant (nonsense)	Lynch syndrome	GPathogenic

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