ClinVar Miner

List of variants in gene RELN reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_005045.4(RELN):c.8046T>C (p.His2682=) rs2229864 0.49951
NM_005045.4(RELN):c.578-3T>C rs607755 0.49658
NM_005045.4(RELN):c.7887T>C (p.Pro2629=) rs56345626 0.17070
NM_005045.4(RELN):c.2989C>G (p.Leu997Val) rs362691 0.10133
NM_005045.4(RELN):c.1776A>G (p.Glu592=) rs2072403 0.09661
NM_005045.4(RELN):c.6702T>C (p.Cys2234=) rs2075043 0.05938
NM_005045.4(RELN):c.1596G>A (p.Gln532=) rs41276154 0.04078
NM_005045.4(RELN):c.5351+3A>G rs6967725 0.03307
NM_005045.4(RELN):c.5831T>G (p.Phe1944Cys) rs77664442 0.02460
NM_005045.4(RELN):c.26A>C (p.Gln9Pro) rs115165703 0.02037
NM_005045.4(RELN):c.7110T>C (p.Val2370=) rs362746 0.01926
NM_005045.4(RELN):c.2932A>G (p.Thr978Ala) rs3025962 0.01491
NM_005045.4(RELN):c.6671+8T>C rs362758 0.01237
NM_005045.4(RELN):c.8086G>A (p.Ala2696Thr) rs115640958 0.01215
NM_005045.4(RELN):c.3839G>A (p.Gly1280Glu) rs55689103 0.01176
NM_005045.4(RELN):c.1799C>T (p.Ser600Phe) rs78008536 0.01065
NM_005045.4(RELN):c.5156C>T (p.Ser1719Leu) rs115913736 0.00515
NM_005045.4(RELN):c.3712A>C (p.Asn1238His) rs114003896 0.00468
NM_005045.4(RELN):c.7086C>T (p.Thr2362=) rs362747 0.00300
NM_005045.4(RELN):c.3651C>G (p.Ile1217Met) rs56342240 0.00287
NM_005045.4(RELN):c.906C>T (p.Ala302=) rs114494558 0.00287
NM_005045.4(RELN):c.416C>G (p.Thr139Ser) rs79471015 0.00283
NM_005045.4(RELN):c.4408G>A (p.Val1470Ile) rs143213152 0.00232
NM_005045.4(RELN):c.7438G>A (p.Gly2480Ser) rs150236371 0.00231
NM_005045.4(RELN):c.1442-8T>C rs181761096 0.00212
NM_005045.4(RELN):c.2303+16G>T rs188276472 0.00198
NM_005045.4(RELN):c.3008+11A>G rs186983114 0.00174
NM_005045.4(RELN):c.246C>G (p.Thr82=) rs113242008 0.00171
NM_005045.4(RELN):c.77C>T (p.Ala26Val) rs144557847 0.00154
NM_005045.4(RELN):c.3477C>A (p.Asn1159Lys) rs114684479 0.00140
NM_005045.4(RELN):c.7181-19A>G rs187689137 0.00127
NM_005045.4(RELN):c.3123C>T (p.Gly1041=) rs41276148 0.00123
NM_005045.4(RELN):c.5880A>G (p.Thr1960=) rs362793 0.00105
NM_005045.4(RELN):c.5200C>G (p.Leu1734Val) rs362800 0.00098
NM_005045.4(RELN):c.6141C>T (p.Phe2047=) rs79161241 0.00098
NM_005045.4(RELN):c.577+7G>T rs188372756 0.00091
NM_005045.4(RELN):c.1035A>G (p.Leu345=) rs113998363 0.00072
NM_005045.4(RELN):c.7644G>A (p.Ser2548=) rs150743664 0.00055
NM_005045.4(RELN):c.3060C>T (p.Asp1020=) rs115886170 0.00026
NM_005045.4(RELN):c.3663C>T (p.Ser1221=) rs199705497 0.00019
NM_005045.4(RELN):c.6302+20C>T rs775229404 0.00019
NM_005045.4(RELN):c.2376T>C (p.Gly792=) rs398124191 0.00016
NM_005045.4(RELN):c.2532G>A (p.Pro844=) rs113842330 0.00016
NM_005045.4(RELN):c.5088T>C (p.Leu1696=) rs114551393 0.00016
NM_005045.4(RELN):c.3009-10G>A rs140358876 0.00014
NM_005045.4(RELN):c.3411C>T (p.Gly1137=) rs137974322 0.00014
NM_005045.4(RELN):c.6553A>T (p.Met2185Leu) rs114686696 0.00010
NM_005045.4(RELN):c.7181-45T>C rs779075555 0.00007
NM_005045.4(RELN):c.5599A>C (p.Arg1867=) rs753376558 0.00004
NM_005045.4(RELN):c.8119+16C>T rs572656670 0.00004
NM_005045.4(RELN):c.8119+17G>A rs377519588 0.00004
NM_005045.4(RELN):c.4314A>T (p.Gly1438=) rs368010584 0.00003
NM_005045.4(RELN):c.5529+10A>T rs371510474 0.00003
NM_005045.4(RELN):c.6888G>A (p.Pro2296=) rs142792443 0.00003
NM_005045.4(RELN):c.330C>T (p.Phe110=) rs1057521487 0.00002
NM_005045.4(RELN):c.5615-16G>A rs1554377679 0.00002
NM_005045.4(RELN):c.5832C>T (p.Phe1944=) rs767598814 0.00002
NM_005045.4(RELN):c.8085C>T (p.Ile2695=) rs138241126 0.00002
NM_005045.4(RELN):c.1092C>T (p.Leu364=) rs142192165 0.00001
NM_005045.4(RELN):c.2442A>G (p.Ser814=) rs759128344 0.00001
NM_005045.4(RELN):c.4719G>A (p.Thr1573=) rs370566453 0.00001
NM_005045.4(RELN):c.4934T>C (p.Ile1645Thr) rs537366000 0.00001
NM_005045.4(RELN):c.5547T>C (p.Leu1849=) rs766701326 0.00001
NM_005045.4(RELN):c.6072+18A>G rs1272084565 0.00001
NM_005045.4(RELN):c.6192C>T (p.His2064=) rs764737797 0.00001
NM_005045.4(RELN):c.6579G>A (p.Lys2193=) rs764925228 0.00001
NM_005045.4(RELN):c.6771G>A (p.Ser2257=) rs367867782 0.00001
NM_005045.4(RELN):c.-24GGC[11] (p.Met1_Glu2insGlyGlyGly) rs55656324
NM_005045.4(RELN):c.1143+15dup rs758452731
NM_005045.4(RELN):c.5797+19T>C rs202190286
NM_005045.4(RELN):c.6523+43_6523+44insTACATTG rs745454190
NM_005045.4(RELN):c.6671+30dup rs150971291
NM_005045.4(RELN):c.7179T>C (p.Tyr2393=) rs1174232635
NM_005045.4(RELN):c.7299C>T (p.Asp2433=) rs1554372988
NM_005045.4(RELN):c.864G>A (p.Lys288=) rs1057523268

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