List of variants in gene MYH3 studied for arthrogryposis multiplex congenita

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_002470.4(MYH3):c.5457+9dup	rs397750512	0.58793
NM_002470.4(MYH3):c.4925A>G (p.Lys1642Arg)	rs143396252	0.00012
NM_002470.4(MYH3):c.5555C>T (p.Thr1852Met)	rs539272823	0.00003
NM_002470.4(MYH3):c.1960-17dup	rs3216884
NM_002470.4(MYH3):c.1960-8del	rs3216884
NM_002470.4(MYH3):c.5457+10dup	rs761191751

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