List of variants reported as uncertain significance for autosomal recessive limb-girdle muscular dystrophy type 2N by Fulgent Genetics, Fulgent Genetics

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_013382.7(POMT2):c.1903G>A (p.Val635Ile)	rs142299878	0.00061
NM_013382.7(POMT2):c.229G>A (p.Asp77Asn)	rs200992827	0.00051
NM_013382.7(POMT2):c.844C>T (p.Arg282Cys)	rs200204831	0.00009
NM_013382.7(POMT2):c.1936G>A (p.Gly646Ser)	rs767592155	0.00006
NM_013382.7(POMT2):c.1106G>A (p.Arg369His)	rs398124260	0.00004
NM_013382.7(POMT2):c.1300C>T (p.Arg434Trp)	rs768256055	0.00002
NM_013382.7(POMT2):c.856C>T (p.Leu286Phe)	rs375363915	0.00002
NM_013382.7(POMT2):c.1274G>C (p.Ser425Thr)	rs774466835	0.00001
NM_013382.7(POMT2):c.1870C>T (p.Arg624Trp)	rs749335757	0.00001
NM_013382.7(POMT2):c.295C>T (p.Arg99Cys)	rs199719668	0.00001
NM_013382.7(POMT2):c.118C>G (p.Arg40Gly)	rs755650000
NM_013382.7(POMT2):c.232G>C (p.Glu78Gln)	rs151103906

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