ClinVar Miner

List of variants reported as benign for SLC35A1-congenital disorder of glycosylation by Invitae

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_006416.5(SLC35A1):c.887-14T>C rs56136150 0.10768
NM_006416.5(SLC35A1):c.7G>T (p.Ala3Ser) rs149903512 0.01248
NM_006416.5(SLC35A1):c.19A>C (p.Asn7His) rs114156788 0.00612
NM_006416.5(SLC35A1):c.16+19G>A rs144960751 0.00007
NM_006416.5(SLC35A1):c.887-9del rs747644865
NM_006416.5(SLC35A1):c.887-9dup rs747644865

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