List of variants reported as uncertain significance for Congenital myopathy 20 by Revvity Omics, Revvity

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001036.6(RYR3):c.6835G>A (p.Val2279Met)	rs41279210	0.00041
NM_001036.6(RYR3):c.12029G>A (p.Arg4010His)	rs202140253	0.00020
NM_001036.6(RYR3):c.11914G>T (p.Asp3972Tyr)
NM_001036.6(RYR3):c.11G>C (p.Gly4Ala)	rs375998723
NM_001036.6(RYR3):c.12785C>A (p.Thr4262Asn)

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