ClinVar Miner

List of variants in gene combination LOC101927870, RELN reported as pathogenic for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_005045.3(RELN):c.10093G>A (p.Val3365Ile) rs115035120
NM_005045.3(RELN):c.8347G>T (p.Gly2783Cys) rs794727997
NM_005045.3(RELN):c.8843+3A>C rs200124755
NM_005045.3(RELN):c.9526G>A (p.Glu3176Lys) rs794727999
NM_005045.3(RELN):c.9976C>T (p.Arg3326Ter) rs751409835

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