List of variants in gene MLH3 reported as likely benign for female reproductive organ cancer

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001040108.2(MLH3):c.4011+15T>G	rs139032600	0.00031
NM_001040108.2(MLH3):c.873T>G (p.Asn291Lys)	rs767413852	0.00009
NM_001040108.2(MLH3):c.149T>A (p.Phe50Tyr)	rs148409389

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