ClinVar Miner

List of variants in gene ALG13 reported as likely benign for History of neurodevelopmental disorder

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Total variants: 7
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HGVS dbSNP
NM_001099922.3(ALG13):c.1211A>C (p.Glu404Ala) rs1569517608
NM_001099922.3(ALG13):c.1591T>C (p.Leu531=) rs112837367
NM_001099922.3(ALG13):c.3084C>T (p.Thr1028=) rs758300150
NM_001099922.3(ALG13):c.3240A>G (p.Pro1080=) rs773452673
NM_001099922.3(ALG13):c.3312A>G (p.Ala1104=) rs1487734085
NM_001099922.3(ALG13):c.354A>G (p.Lys118=) rs1569510723
NM_001099922.3(ALG13):c.975T>G (p.Thr325=) rs767735916

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