ClinVar Miner

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

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_005045.4(RELN):c.10020G>A (p.Ser3340=) rs760919496
NM_005045.4(RELN):c.10108A>G (p.Thr3370Ala) rs570807790
NM_005045.4(RELN):c.8154A>T (p.Thr2718=) rs1554367205
NM_005045.4(RELN):c.8625G>A (p.Pro2875=) rs190273964
NM_005045.4(RELN):c.8863C>T (p.Arg2955Cys) rs114501042
NM_005045.4(RELN):c.8951-11_8951-8dup rs1554364085
NM_005045.4(RELN):c.9105G>A (p.Gly3035=) rs1279644782
NM_005045.4(RELN):c.9172T>C (p.Leu3058=) rs2286261
NM_005045.4(RELN):c.9414C>T (p.Ser3138=) rs375427974
NM_005045.4(RELN):c.9825C>T (p.Ser3275=) rs149713137
NM_005045.4(RELN):c.9984-9G>A rs758320422

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