List of variants in gene combination LOC129933707, MSH6 reported as uncertain significance for carcinoma

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.257C>T (p.Thr86Ile)	rs768444916	0.00002
NM_000179.3(MSH6):c.248C>A (p.Ala83Asp)	rs876661197
NM_000179.3(MSH6):c.254CCA[1] (p.Thr86del)	rs1553408448
NM_000179.3(MSH6):c.260G>C (p.Ser87Thr)	rs1114167734

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