ClinVar Miner

List of variants in gene RELN studied for Familial temporal lobe epilepsy 1; Norman-Roberts syndrome; Epilepsy, familial temporal lobe, 7

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Total variants: 29
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HGVS dbSNP
NM_005045.4(RELN):c.1001G>A (p.Arg334His) rs146922726
NM_005045.4(RELN):c.1108G>C (p.Gly370Arg) rs143050366
NM_005045.4(RELN):c.1231C>A (p.Leu411Ile) rs144978163
NM_005045.4(RELN):c.1336G>C (p.Glu446Gln) rs56146903
NM_005045.4(RELN):c.139G>A (p.Glu47Lys) rs139648092
NM_005045.4(RELN):c.1483A>G (p.Ile495Val) rs150850005
NM_005045.4(RELN):c.1817C>T (p.Thr606Ile) rs540111252
NM_005045.4(RELN):c.2015C>T (p.Pro672Leu) rs201044262
NM_005045.4(RELN):c.2125A>G (p.Met709Val) rs114577182
NM_005045.4(RELN):c.2446C>T (p.Leu816Phe) rs144653976
NM_005045.4(RELN):c.2954C>G (p.Ala985Gly) rs138598422
NM_005045.4(RELN):c.3197C>T (p.Pro1066Leu) rs116225248
NM_005045.4(RELN):c.4337A>G (p.Asn1446Ser) rs115577014
NM_005045.4(RELN):c.4495G>C (p.Asp1499His) rs200428576
NM_005045.4(RELN):c.4907A>G (p.Asp1636Gly) rs587780439
NM_005045.4(RELN):c.5095G>A (p.Glu1699Lys) rs147657490
NM_005045.4(RELN):c.5225G>A (p.Arg1742Gln) rs199553777
NM_005045.4(RELN):c.5468C>A (p.Ala1823Glu) rs1244373166
NM_005045.4(RELN):c.5668A>G (p.Ile1890Val) rs147026512
NM_005045.4(RELN):c.5711C>T (p.Thr1904Met) rs114190729
NM_005045.4(RELN):c.5822T>C (p.Val1941Ala) rs149837553
NM_005045.4(RELN):c.59C>T (p.Thr20Met) rs145135688
NM_005045.4(RELN):c.6193G>A (p.Val2065Ile) rs201627577
NM_005045.4(RELN):c.6520G>A (p.Glu2174Lys) rs146877597
NM_005045.4(RELN):c.6647G>A (p.Arg2216Gln) rs200010849
NM_005045.4(RELN):c.6726G>C (p.Arg2242Ser) rs201422815
NM_005045.4(RELN):c.6925G>A (p.Asp2309Asn) rs138978280
NM_005045.4(RELN):c.697G>A (p.Ala233Thr) rs181961566
NM_005045.4(RELN):c.8005G>A (p.Val2669Ile) rs375985673

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