List of variants in gene MYH3 reported as benign for Distal arthrogryposis type 2B1

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: 31

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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.1581+13A>C	rs2285468	0.63294
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.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.3348T>C (p.Ile1116=)	rs201626	0.14064
NM_002470.4(MYH3):c.2106C>T (p.Gly702=)	rs56259391	0.05968
NM_002470.4(MYH3):c.2610A>G (p.Lys870=)	rs56163389	0.05967
NM_002470.4(MYH3):c.5457+3G>A	rs200954595	0.02449
NM_002470.4(MYH3):c.6T>C (p.Ser2=)	rs17817203	0.02219
NM_002470.4(MYH3):c.3008C>T (p.Ala1003Val)	rs34088014	0.02195
NM_002470.4(MYH3):c.4155A>G (p.Glu1385=)	rs58343499	0.02173
NM_002470.4(MYH3):c.3938C>T (p.Thr1313Ile)	rs35230241	0.02138
NM_002470.4(MYH3):c.4128C>T (p.Tyr1376=)	rs112569418	0.01571
NM_002470.4(MYH3):c.699C>T (p.Asn233=)	rs16943604	0.01272
NM_002470.4(MYH3):c.349-7C>T	rs114366800	0.01261
NM_002470.4(MYH3):c.3009G>A (p.Ala1003=)	rs61735353	0.01244
NM_002470.4(MYH3):c.774G>A (p.Lys258=)	rs16943598	0.00793
NM_002470.4(MYH3):c.3726T>C (p.Ser1242=)	rs77946261	0.00792
NM_002470.4(MYH3):c.3592G>A (p.Ala1198Thr)	rs61735358	0.00641
NM_002470.4(MYH3):c.453C>T (p.Ala151=)	rs7214436	0.00621
NM_002470.4(MYH3):c.1575C>T (p.Ile525=)	rs34695778	0.00528
NM_002470.4(MYH3):c.2683-4T>C	rs182229640	0.00350
NM_002470.4(MYH3):c.3409C>T (p.Arg1137Cys)	rs12941197	0.00245
NM_002470.4(MYH3):c.3138A>C (p.Arg1046=)	rs2285475
NM_002470.4(MYH3):c.3445G>C (p.Glu1149Gln)	rs145785711
NM_002470.4(MYH3):c.5254G>A (p.Ala1752Thr)	rs34393601

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