List of variants in gene MYH9 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 16

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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.3345A>G (p.Glu1115=)	rs875725	0.03292
NM_002473.6(MYH9):c.3100+11G>C	rs41279999	0.02869
NM_002473.6(MYH9):c.3838-8C>T	rs145429636	0.02315
NM_002473.6(MYH9):c.1108+9C>T	rs145751072	0.00959
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.5181G>A (p.Leu1727=)	rs115170675	0.00292
NM_002473.6(MYH9):c.5818G>A (p.Gly1940Arg)	rs140588099	0.00156
NM_002473.6(MYH9):c.4727G>A (p.Arg1576Gln)	rs143269195	0.00088
NM_002473.6(MYH9):c.3192C>T (p.Ile1064=)	rs144807538	0.00076
NM_002473.6(MYH9):c.4344+10C>T	rs200977419	0.00061
NM_002473.6(MYH9):c.5483+4C>G	rs56327920
NM_002473.6(MYH9):c.5766-3del	rs141686520
NM_002473.6(MYH9):c.5781G>T (p.Pro1927=)	rs80050551

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