"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "LOC129933707"[ - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 492704	NM_000179.3(MSH6):c.260+2T>A	LOC129933707, MSH6	Single nucleotide variant (splice donor variant +1 more)	Lynch syndrome	GLikely pathogenic
Select item 492705	NM_000179.3(MSH6):c.260+3A>G	LOC129933707, MSH6	Single nucleotide variant (intron variant)	Hereditary nonpolyposis colorectal neoplasms	GUncertain significance
Select item 89295	NM_000179.3(MSH6):c.260+22C>G	LOC129933707, MSH6	Single nucleotide variant (intron variant)	Lynch syndrome	GBenign

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