ClinVar Miner

List of variants reported as likely pathogenic for SLC35A1-congenital disorder of glycosylation

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006416.5(SLC35A1):c.133A>G (p.Thr45Ala)	rs145006535	0.00306
NM_006416.5(SLC35A1):c.467C>G (p.Thr156Arg)	rs578205635
NM_006416.5(SLC35A1):c.586G>A (p.Glu196Lys)	rs1554166844

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