ClinVar Miner

List of variants in gene GCNT2 reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_145649.5(GCNT2):c.*1022_*1025dup rs139647870 0.07101
NM_145655.3(GCNT2):c.*2765C>T rs9460953 0.01750
NM_145649.5(GCNT2):c.*1112G>A rs6899538 0.00398
NM_145649.5(GCNT2):c.*196A>G rs77170997 0.00354
NM_001491.3(GCNT2):c.630T>G (p.Gly210=) rs148372193 0.00167
NM_145649.5(GCNT2):c.*93G>A rs556902601 0.00108
NM_145649.5(GCNT2):c.*2174G>A rs539707774 0.00011
NM_145649.5(GCNT2):c.*1432C>A rs578022959
NM_145649.5(GCNT2):c.*2330G>T rs145879560
NM_145649.5(GCNT2):c.*2521C>T rs190656787

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