List of variants reported as uncertain significance for Muscular dystrophy, limb-girdle, autosomal recessive 23 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000426.4(LAMA2):c.6322C>T (p.Arg2108Trp)	rs139824017	0.00012
NM_000426.4(LAMA2):c.1085G>T (p.Arg362Ile)	rs182958473	0.00005
NM_000426.4(LAMA2):c.2585G>A (p.Cys862Tyr)	rs2482291953
NM_000426.4(LAMA2):c.2749+4_2749+15del	rs2482293091
NM_000426.4(LAMA2):c.29T>A (p.Leu10His)	rs2482366909

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