ClinVar Miner

List of variants reported as uncertain significance for Lennox-Gastaut syndrome by Mendelics

Included ClinVar conditions (6):

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 4

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HGVS	dbSNP
NM_001271.4(CHD2):c.4173dup (p.Gln1392fs)	rs749969667
NM_001271.4(CHD2):c.4435G>A (p.Val1479Met)
NM_004408.4(DNM1):c.112G>A (p.Gly38Ser)	rs1131692025
NM_004408.4(DNM1):c.985C>G (p.Leu329Val)

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