List of variants in gene MLH3 reported as uncertain significance for Lynch syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001040108.2(MLH3):c.3440A>T (p.Asn1147Ile)	rs142124529	0.00035
NM_001040108.2(MLH3):c.*1701del	rs886050770
NM_001040108.2(MLH3):c.*3048del	rs886050767
NM_001040108.2(MLH3):c.*797dup	rs886050773
NM_001040108.2(MLH3):c.957_958delinsAT	rs386778871
NM_001040108.2(MLH3):c.-63-10dup	rs886050781

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