List of variants in gene MSH6 reported as uncertain significance by True Health Diagnostics

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.3647-6T>A	rs182871847	0.00134
NM_000179.3(MSH6):c.2561A>T (p.Lys854Met)	rs34374438	0.00036
NM_000179.3(MSH6):c.3727A>T (p.Thr1243Ser)	rs147453999	0.00009
NM_000179.3(MSH6):c.1898C>G (p.Thr633Ser)	rs1553413271
NM_000179.3(MSH6):c.347A>G (p.Asp116Gly)	rs1553410255
NM_000179.3(MSH6):c.3758T>C (p.Val1253Ala)	rs202066386
NM_000179.3(MSH6):c.905G>C (p.Arg302Thr)	rs587781510

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