ClinVar Miner

List of variants in gene RELN reported as 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: 45
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HGVS dbSNP
NM_005045.3(RELN):c.1075G>A (p.Val359Ile) rs114926265
NM_005045.3(RELN):c.1290-3delT rs146986040
NM_005045.3(RELN):c.1290-3dupT rs146986040
NM_005045.3(RELN):c.1377G>A (p.Arg459=) rs73712207
NM_005045.3(RELN):c.1442-8T>C rs181761096
NM_005045.3(RELN):c.1596G>A (p.Gln532=) rs41276154
NM_005045.3(RELN):c.1799C>T (p.Ser600Phe) rs78008536
NM_005045.3(RELN):c.1824C>T (p.Cys608=) rs79620906
NM_005045.3(RELN):c.1888A>C (p.Ser630Arg) rs115734214
NM_005045.3(RELN):c.246C>G (p.Thr82=) rs113242008
NM_005045.3(RELN):c.26A>C (p.Gln9Pro) rs115165703
NM_005045.3(RELN):c.2932A>G (p.Thr978Ala) rs3025962
NM_005045.3(RELN):c.3060C>T (p.Asp1020=) rs115886170
NM_005045.3(RELN):c.3123C>T (p.Gly1041=) rs41276148
NM_005045.3(RELN):c.3424T>A (p.Ser1142Thr) rs145484343
NM_005045.3(RELN):c.3839G>A (p.Gly1280Glu) rs55689103
NM_005045.3(RELN):c.416C>G (p.Thr139Ser) rs79471015
NM_005045.3(RELN):c.4182A>G (p.Ser1394=) rs147496823
NM_005045.3(RELN):c.4408G>A (p.Val1470Ile) rs143213152
NM_005045.3(RELN):c.4589-8T>G rs362801
NM_005045.3(RELN):c.4937-5_4937-4dup rs35268159
NM_005045.3(RELN):c.4986C>G (p.Thr1662=) rs78221963
NM_005045.3(RELN):c.5088T>C (p.Leu1696=) rs114551393
NM_005045.3(RELN):c.5108C>G (p.Pro1703Arg) rs2229860
NM_005045.3(RELN):c.5156C>T (p.Ser1719Leu) rs115913736
NM_005045.3(RELN):c.5284G>A (p.Val1762Ile) rs79499902
NM_005045.3(RELN):c.5351+3A>G rs6967725
NM_005045.3(RELN):c.5618C>T (p.Thr1873Ile) rs41275239
NM_005045.3(RELN):c.565C>T (p.His189Tyr) rs115806540
NM_005045.3(RELN):c.5775A>G (p.Arg1925=) rs2711866
NM_005045.3(RELN):c.5831T>G (p.Phe1944Cys) rs77664442
NM_005045.3(RELN):c.5880A>G (p.Thr1960=) rs362793
NM_005045.3(RELN):c.6078C>T (p.Asn2026=) rs79610081
NM_005045.3(RELN):c.6084C>T (p.Gly2028=) rs114019779
NM_005045.3(RELN):c.621C>T (p.Asp207=) rs114627891
NM_005045.3(RELN):c.6228C>T (p.Ser2076=) rs115379833
NM_005045.3(RELN):c.6343G>A (p.Gly2115Ser) rs116716038
NM_005045.3(RELN):c.6671+8T>C rs362758
NM_005045.3(RELN):c.7086C>T (p.Thr2362=) rs362747
NM_005045.3(RELN):c.7110T>C (p.Val2370=) rs362746
NM_005045.3(RELN):c.7110_7111invTG (p.Ala2371Thr)
NM_005045.3(RELN):c.7438G>A (p.Gly2480Ser) rs150236371
NM_005045.3(RELN):c.7538C>G (p.Ser2513Cys) rs114647348
NM_005045.3(RELN):c.8086G>A (p.Ala2696Thr) rs115640958
NM_005045.3(RELN):c.906C>T (p.Ala302=) rs114494558

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