List of variants in gene MYH9 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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_002473.6(MYH9):c.4396C>T (p.Arg1466Trp)	rs139134727	0.00195
NM_002473.6(MYH9):c.4817C>T (p.Ser1606Leu)	rs145319741	0.00009
NM_002473.6(MYH9):c.1561C>T (p.Pro521Ser)	rs1452533167
NM_002473.6(MYH9):c.3451A>G (p.Thr1151Ala)	rs2146338652
NM_002473.6(MYH9):c.4542T>G (p.Asp1514Glu)	rs1445705225
NM_002473.6(MYH9):c.4679T>G (p.Val1560Gly)	rs1064794326
NM_002473.6(MYH9):c.467C>G (p.Thr156Ser)	rs931698088

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