ClinVar Miner

List of variants reported as uncertain significance for Miyoshi muscular dystrophy 1; Autosomal recessive limb-girdle muscular dystrophy type 2B; Myopathy, distal, with anterior tibial onset by Fulgent Genetics,Fulgent Genetics

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Total variants: 3

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HGVS	dbSNP
NM_001130987.2(DYSF):c.1618T>C (p.Tyr540His)	rs777489323
NM_001130987.2(DYSF):c.2335G>A (p.Gly779Ser)	rs138654170
NM_001130987.2(DYSF):c.3695C>T (p.Pro1232Leu)	rs150942486

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