List of variants in gene MLH1 reported as likely benign for breast disorder

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000249.4(MLH1):c.375A>G (p.Ala125=)	rs1800144	0.00062
NM_000249.4(MLH1):c.702G>A (p.Glu234=)	rs35908749	0.00041
NM_000249.4(MLH1):c.65G>C (p.Gly22Ala)	rs41295280	0.00016
NM_000249.4(MLH1):c.1808C>G (p.Pro603Arg)	rs63750876	0.00009
NM_000249.4(MLH1):c.42A>C (p.Thr14=)	rs369737664	0.00007
NM_000249.4(MLH1):c.545+10A>C	rs781569222	0.00001
NM_000249.4(MLH1):c.1039-8_1039-7insTA	rs535965616
NM_000249.4(MLH1):c.2091C>T (p.Leu697=)	rs536488280
NM_000249.4(MLH1):c.2247A>G (p.Leu749=)	rs786202209
NM_000249.4(MLH1):c.864A>C (p.Thr288=)	rs1457205659
NM_000249.4(MLH1):c.927C>T (p.Pro309=)	rs63749896

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