List of variants reported as likely benign for ALG6-congenital disorder of glycosylation 1C by Illumina Laboratory Services, Illumina

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_013339.4(ALG6):c.391T>C (p.Tyr131His)	rs35383149	0.02935
NM_013339.4(ALG6):c.1357C>G (p.Leu453Val)	rs41285372	0.01295
NM_013339.4(ALG6):c.*268C>T	rs114111123	0.01221
NM_013339.4(ALG6):c.-121T>G	rs116034504	0.00994
NM_013339.4(ALG6):c.*1415T>G	rs148327539	0.00827
NM_013339.4(ALG6):c.*1434T>C	rs141443584	0.00822
NM_013339.4(ALG6):c.1323T>C (p.Tyr441=)	rs116660078	0.00791
NM_013339.4(ALG6):c.751A>G (p.Thr251Ala)	rs61755863	0.00705
NM_013339.4(ALG6):c.*1136C>T	rs143324400	0.00429
NM_013339.4(ALG6):c.*961C>T	rs144020923	0.00415
NM_013339.4(ALG6):c.1452C>T (p.Phe484=)	rs150298974	0.00044

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