Variants in gene MLH3 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
NM_001040108.2(MLH3):c.1870G>C (p.Glu624Gln)	rs28756986	0.00772
NM_001040108.2(MLH3):c.2490T>G (p.Phe830Leu)	rs114015611	0.00177
NM_001040108.2(MLH3):c.1939C>T (p.Arg647Cys)	rs28756987	0.00171
NM_001040108.2(MLH3):c.4351G>A (p.Glu1451Lys)	rs28939071	0.00104
NM_001040108.2(MLH3):c.3488G>A (p.Gly1163Asp)	rs28757011	0.00100
NM_001040108.2(MLH3):c.423C>T (p.Ser141=)	rs142179277	0.00100
NM_001040108.2(MLH3):c.2838C>A (p.Ser946=)	rs181990057	0.00073
NM_001040108.2(MLH3):c.2911G>A (p.Val971Ile)	rs41555714	0.00048
NM_001040108.2(MLH3):c.2373G>A (p.Leu791=)	rs764724825	0.00004
NM_001040108.2(MLH3):c.4032C>T (p.Gly1344=)	rs565238806	0.00004
NM_001040108.2(MLH3):c.149T>A (p.Phe50Tyr)	rs148409389
NM_001040108.2(MLH3):c.2221G>A (p.Val741Ile)	rs28756990

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