List of variants in gene MYH3 reported as benign for autosomal recessive disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_002470.4(MYH3):c.4957-16G>C	rs2239936	0.78067
NM_002470.4(MYH3):c.3574G>A (p.Ala1192Thr)	rs2285477	0.69723
NM_002470.4(MYH3):c.1581+13A>C	rs2285468	0.63294
NM_002470.4(MYH3):c.534-44T>C	rs1989810	0.63169
NM_002470.4(MYH3):c.5457+9dup	rs397750512	0.58793
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.2166-15A>G	rs876660	0.57314
NM_002470.4(MYH3):c.1141+32G>A	rs2239934	0.57301
NM_002470.4(MYH3):c.2916A>G (p.Thr972=)	rs2285472	0.57294
NM_002470.4(MYH3):c.2926-12A>G	rs2285473	0.57289
NM_002470.4(MYH3):c.2952T>C (p.Ser984=)	rs2285474	0.57288
NM_002470.4(MYH3):c.4956+32C>T	rs4792008	0.57288
NM_002470.4(MYH3):c.1003-22C>T	rs2239933	0.57286
NM_002470.4(MYH3):c.349-43C>T	rs2285466	0.57166
NM_002470.4(MYH3):c.349-36A>G	rs2285467	0.12931
NM_002470.4(MYH3):c.1960-8del	rs3216884
NM_002470.4(MYH3):c.2682+30_2682+31del	rs34274020
NM_002470.4(MYH3):c.3138A>C (p.Arg1046=)	rs2285475
NM_002470.4(MYH3):c.5796+30C>T	rs12940161
NM_002470.4(MYH3):c.643-43dup	rs3214114

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