List of variants in gene MSH6 reported as uncertain significance for breast carcinoma

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.3893A>G (p.Tyr1298Cys)	rs786202520	0.00001
NM_000179.3(MSH6):c.3259C>T (p.Pro1087Ser)	rs63750998
NM_000179.3(MSH6):c.3646+5G>A	rs1669974239
NM_000179.3(MSH6):c.3969T>G (p.Phe1323Leu)	rs1057520473

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