ClinVar Miner

List of variants reported as likely benign for Congenital glucose-galactose malabsorption by Illumina Laboratory Services, Illumina

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Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_000343.4(SLC5A1):c.*1203A>G rs149444431 0.00762
NM_000343.4(SLC5A1):c.*1476A>G rs190638859 0.00277
NM_000343.4(SLC5A1):c.1846G>A (p.Gly616Ser) rs61733910 0.00081
NM_000343.4(SLC5A1):c.1200C>T (p.Ser400=) rs142046439 0.00027
NM_000343.4(SLC5A1):c.744C>T (p.Asn248=) rs185126699 0.00026
NM_000343.4(SLC5A1):c.*1237A>G rs368732312 0.00016
NM_000343.4(SLC5A1):c.*1455C>A rs559383534 0.00010
NM_000343.3(SLC5A1):c.-36G>A rs200961861 0.00002
NM_000343.4(SLC5A1):c.373-13G>A rs201398293 0.00001
NM_000343.4(SLC5A1):c.*423dup rs140860103

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