List of variants in gene combination LOC126862493, MYH8, MYHAS reported as uncertain significance for arthrogryposis syndrome

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002472.3(MYH8):c.5459C>T (p.Ala1820Val)	rs148625172	0.00088
NM_002472.3(MYH8):c.5539G>A (p.Glu1847Lys)	rs757938047	0.00013
NM_002472.3(MYH8):c.5543G>A (p.Arg1848Gln)	rs376732590	0.00005

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