List of variants in gene combination LOC129933707, MSH6 reported as likely pathogenic by Labcorp Genetics (formerly Invitae), Labcorp

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_000179.3(MSH6):c.260+1G>C	rs1553408467
NM_000179.3(MSH6):c.260+2T>C	rs1553408469
NM_000179.3(MSH6):c.260+2_260+3delinsAG	rs1064794075

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