ClinVar Miner

List of variants reported as uncertain significance for ALG3-congenital disorder of glycosylation by Baylor Genetics

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_005787.6(ALG3):c.1084G>A (p.Val362Ile) rs186946267 0.00068
NM_001006941.2(ALG3):c.46G>T (p.Gly16Trp) rs373046727
NM_005787.6(ALG3):c.296+5G>A rs1719108178
NM_005787.6(ALG3):c.626T>C (p.Met209Thr) rs1553828467
NM_005787.6(ALG3):c.985C>G (p.Pro329Ala) rs751758378

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