List of variants in gene MYH9 reported as benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_002473.6(MYH9):c.3429T>G (p.Ala1143=)	rs710181	0.97278
NM_002473.6(MYH9):c.1728+10G>A	rs2413396	0.77118
NM_002473.6(MYH9):c.4876A>G (p.Ile1626Val)	rs2269529	0.17342
NM_002473.6(MYH9):c.4872G>T (p.Ala1624=)	rs2269530	0.17309
NM_002473.6(MYH9):c.3100+11G>C	rs41279999	0.02869
NM_002473.6(MYH9):c.3838-12C>T	rs113698937	0.01529
NM_002473.6(MYH9):c.1626C>T (p.Phe542=)	rs7285745	0.01011
NM_002473.6(MYH9):c.136C>T (p.Leu46Phe)	rs147122501	0.00554
NM_002473.6(MYH9):c.1083C>T (p.Asp361=)	rs56001030	0.00436
NM_002473.6(MYH9):c.5781G>T (p.Pro1927=)	rs80050551

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