ClinVar Miner

List of variants reported as uncertain significance for Lennox-Gastaut syndrome by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_000814.6(GABRB3):c.292G>A (p.Ala98Thr) rs756369937
NM_000814.6(GABRB3):c.557C>T (p.Thr186Met) rs769801846
NM_001271.4(CHD2):c.2973G>A (p.Gln991=) rs903186613
NM_001271.4(CHD2):c.4061G>A (p.Arg1354Lys) rs370160870
NM_001271.4(CHD2):c.5069G>A (p.Arg1690Gln) rs564787975
NM_001271.4(CHD2):c.881G>T (p.Gly294Val) rs771390521

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