List of variants in gene combination LOC129933707, MSH6 reported as pathogenic for colorectal cancer

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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.215_258del (p.Leu72fs)	rs1553408380
NM_000179.3(MSH6):c.246dup (p.Ala83fs)	rs1668136752
NM_000179.3(MSH6):c.255del (p.Thr86fs)	rs1064793183

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