ClinVar Miner

List of variants in gene 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: 53
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HGVS dbSNP
NM_005045.3(RELN):c.1555G>T (p.Val519Phe) rs560704715
NM_005045.3(RELN):c.2016G>A (p.Pro672=) rs146749232
NM_005045.3(RELN):c.2352G>A (p.Thr784=) rs148510862
NM_005045.3(RELN):c.2376T>C (p.Gly792=) rs398124191
NM_005045.3(RELN):c.2466-6C>T rs1167948188
NM_005045.3(RELN):c.2754A>G (p.Gln918=) rs114620008
NM_005045.3(RELN):c.2827C>T (p.His943Tyr) rs190615928
NM_005045.3(RELN):c.3477C>A (p.Asn1159Lys) rs114684479
NM_005045.3(RELN):c.3483G>A (p.Gly1161=) rs1254504314
NM_005045.3(RELN):c.3642C>T (p.Val1214=) rs151252449
NM_005045.3(RELN):c.3651C>G (p.Ile1217Met) rs56342240
NM_005045.3(RELN):c.3786A>G (p.Gly1262=) rs577453361
NM_005045.3(RELN):c.3891T>A (p.Pro1297=) rs145600583
NM_005045.3(RELN):c.3913-9T>C rs372473867
NM_005045.3(RELN):c.408G>C (p.Leu136=) rs1554427416
NM_005045.3(RELN):c.4191C>T (p.Asn1397=) rs544646610
NM_005045.3(RELN):c.4230G>A (p.Glu1410=) rs184601053
NM_005045.3(RELN):c.4257T>C (p.His1419=) rs138924805
NM_005045.3(RELN):c.4720G>A (p.Ala1574Thr) rs78480723
NM_005045.3(RELN):c.474-7T>C rs55693709
NM_005045.3(RELN):c.5016T>C (p.Cys1672=) rs983510937
NM_005045.3(RELN):c.5145A>G (p.Ser1715=) rs113229231
NM_005045.3(RELN):c.5200C>G (p.Leu1734Val) rs362800
NM_005045.3(RELN):c.5274G>T (p.Ala1758=) rs139102992
NM_005045.3(RELN):c.5352-9C>G rs758405612
NM_005045.3(RELN):c.5529+10A>T rs371510474
NM_005045.3(RELN):c.5599A>C (p.Arg1867=) rs753376558
NM_005045.3(RELN):c.5643G>A (p.Leu1881=) rs141387255
NM_005045.3(RELN):c.577+9T>C rs750186579
NM_005045.3(RELN):c.5796C>T (p.Asn1932=) rs200299096
NM_005045.3(RELN):c.5923G>A (p.Gly1975Ser) rs114807343
NM_005045.3(RELN):c.6072+7G>T rs777197865
NM_005045.3(RELN):c.6141C>T (p.Phe2047=) rs79161241
NM_005045.3(RELN):c.6147G>A (p.Ala2049=) rs116750302
NM_005045.3(RELN):c.6213C>T (p.Thr2071=) rs554215103
NM_005045.3(RELN):c.6240C>T (p.Tyr2080=) rs201505136
NM_005045.3(RELN):c.6303-9C>T rs200658237
NM_005045.3(RELN):c.6429C>T (p.Ile2143=) rs1554374836
NM_005045.3(RELN):c.6471A>G (p.Pro2157=) rs370086835
NM_005045.3(RELN):c.6553A>T (p.Met2185Leu) rs114686696
NM_005045.3(RELN):c.656+7dup rs768445353
NM_005045.3(RELN):c.6939T>C (p.Ile2313=) rs113498433
NM_005045.3(RELN):c.6962C>T (p.Thr2321Met) rs116065504
NM_005045.3(RELN):c.7107C>T (p.Asp2369=) rs114339919
NM_005045.3(RELN):c.7128C>G (p.Ser2376=) rs116057819
NM_005045.3(RELN):c.7180+8T>C rs1022021889
NM_005045.3(RELN):c.7287C>A (p.Ile2429=) rs915583909
NM_005045.3(RELN):c.7644G>A (p.Ser2548=) rs150743664
NM_005045.3(RELN):c.7713T>C (p.Asn2571=) rs1359170573
NM_005045.3(RELN):c.77C>T (p.Ala26Val) rs144557847
NM_005045.3(RELN):c.8004C>T (p.Thr2668=) rs368087558
NM_005045.3(RELN):c.8028C>T (p.Ser2676=) rs777057396
NM_005045.3(RELN):c.877G>A (p.Asp293Asn) rs200289289

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