List of variants in gene combination LOC129933707, MSH6 reported as uncertain significance for not specified

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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: 5

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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.260+7G>A	rs774479750	0.00001
NM_000179.3(MSH6):c.247G>A (p.Ala83Thr)	rs755964436
NM_000179.3(MSH6):c.260+11G>T	rs550120121
NM_000179.3(MSH6):c.260+5C>T	rs1440012800

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