List of variants in gene MYH3 reported as benign 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_002470.4(MYH3):c.3574G>A (p.Ala1192Thr)	rs2285477	0.69723
NM_002470.4(MYH3):c.2151C>A (p.Gly717=)	rs876657	0.58590
NM_002470.4(MYH3):c.4731C>T (p.Ile1577=)	rs2285479	0.57510
NM_002470.4(MYH3):c.2532A>G (p.Ala844=)	rs2285469	0.57316
NM_002470.4(MYH3):c.2916A>G (p.Thr972=)	rs2285472	0.57294
NM_002470.4(MYH3):c.2952T>C (p.Ser984=)	rs2285474	0.57288
NM_002470.4(MYH3):c.3348T>C (p.Ile1116=)	rs201626	0.14064
NM_002470.4(MYH3):c.774G>A (p.Lys258=)	rs16943598	0.00793
NM_002470.4(MYH3):c.4172+9C>T	rs116028239	0.00364
NM_002470.4(MYH3):c.4910C>T (p.Ala1637Val)	rs34165480	0.00311
NM_002470.4(MYH3):c.252G>A (p.Lys84=)	rs147410236	0.00156
NM_002470.4(MYH3):c.3138A>C (p.Arg1046=)	rs2285475

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