ClinVar Miner

List of variants in gene RELN reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_005045.4(RELN):c.6084C>T (p.Gly2028=) rs114019779 0.00507
NM_005045.4(RELN):c.5108C>G (p.Pro1703Arg) rs2229860 0.00361
NM_005045.4(RELN):c.5923G>A (p.Gly1975Ser) rs114807343 0.00300
NM_005045.4(RELN):c.6228C>T (p.Ser2076=) rs115379833 0.00291
NM_005045.4(RELN):c.3651C>G (p.Ile1217Met) rs56342240 0.00287
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.3477C>A (p.Asn1159Lys) rs114684479 0.00140
NM_005045.4(RELN):c.3123C>T (p.Gly1041=) rs41276148 0.00123
NM_005045.4(RELN):c.3424T>A (p.Ser1142Thr) rs145484343 0.00114
NM_005045.4(RELN):c.474-7T>C rs55693709 0.00105
NM_005045.4(RELN):c.5880A>G (p.Thr1960=) rs362793 0.00105
NM_005045.4(RELN):c.6141C>T (p.Phe2047=) rs79161241 0.00098
NM_005045.4(RELN):c.1001G>A (p.Arg334His) rs146922726 0.00091
NM_005045.4(RELN):c.4182A>G (p.Ser1394=) rs147496823 0.00080
NM_005045.4(RELN):c.6939T>C (p.Ile2313=) rs113498433 0.00054
NM_005045.4(RELN):c.5822T>C (p.Val1941Ala) rs149837553 0.00041
NM_005045.4(RELN):c.5136G>A (p.Thr1712=) rs147933593 0.00038
NM_005045.4(RELN):c.5095G>A (p.Glu1699Lys) rs147657490 0.00032
NM_005045.4(RELN):c.4275A>G (p.Gly1425=) rs141617635 0.00031
NM_005045.4(RELN):c.5643G>A (p.Leu1881=) rs141387255 0.00029
NM_005045.4(RELN):c.2868C>T (p.His956=) rs362694 0.00026
NM_005045.4(RELN):c.5088T>C (p.Leu1696=) rs114551393 0.00016
NM_005045.4(RELN):c.227-6T>C rs769480867 0.00014
NM_005045.4(RELN):c.7268G>A (p.Arg2423His) rs140660860 0.00012
NM_005045.4(RELN):c.5274G>T (p.Ala1758=) rs139102992 0.00010
NM_005045.4(RELN):c.576A>G (p.Leu192=) rs142874980 0.00009
NM_005045.4(RELN):c.6170T>G (p.Leu2057Arg) rs138909076 0.00006
NM_005045.4(RELN):c.7035C>T (p.Pro2345=) rs906374670 0.00004
NM_005045.4(RELN):c.2566A>G (p.Ile856Val) rs371309082 0.00002
NM_005045.4(RELN):c.4654A>G (p.Met1552Val) rs558308794 0.00002
NM_005045.4(RELN):c.5013C>A (p.Gly1671=) rs758902738 0.00002
NM_005045.4(RELN):c.6106G>A (p.Ala2036Thr) rs371614773 0.00002
NM_005045.4(RELN):c.8004C>T (p.Thr2668=) rs368087558 0.00002
NM_005045.4(RELN):c.8085C>T (p.Ile2695=) rs138241126 0.00002
NM_005045.4(RELN):c.2442A>G (p.Ser814=) rs759128344 0.00001
NM_005045.4(RELN):c.2976G>A (p.Arg992=) rs1250895278 0.00001
NM_005045.4(RELN):c.4041C>T (p.Cys1347=) rs762723785 0.00001
NM_005045.4(RELN):c.4719G>A (p.Thr1573=) rs370566453 0.00001
NM_005045.4(RELN):c.5571A>G (p.Thr1857=) rs374234799 0.00001
NM_005045.4(RELN):c.5730T>C (p.Asn1910=) rs761717557 0.00001
NM_005045.4(RELN):c.7743T>C (p.Tyr2581=) rs1316095724 0.00001
NM_005045.4(RELN):c.7762A>C (p.Asn2588His) rs569919781 0.00001
NM_005045.4(RELN):c.-24GGC[4] rs55656324
NM_005045.4(RELN):c.1227A>G (p.Val409=)
NM_005045.4(RELN):c.1248T>G (p.Ile416Met)
NM_005045.4(RELN):c.1526T>G (p.Leu509Arg)
NM_005045.4(RELN):c.2493T>C (p.Asp831=)
NM_005045.4(RELN):c.3468G>A (p.Gln1156=)
NM_005045.4(RELN):c.3609G>A (p.Val1203=)
NM_005045.4(RELN):c.4485G>T (p.Thr1495=) rs542018962
NM_005045.4(RELN):c.4752G>A (p.Lys1584=)
NM_005045.4(RELN):c.5085T>C (p.His1695=)
NM_005045.4(RELN):c.5712G>A (p.Thr1904=) rs1293070633
NM_005045.4(RELN):c.588T>C (p.His196=)
NM_005045.4(RELN):c.6000A>G (p.Ser2000=) rs1554376650
NM_005045.4(RELN):c.6288G>A (p.Lys2096=) rs1345151350
NM_005045.4(RELN):c.7764C>T (p.Asn2588=)
NM_005045.4(RELN):c.7827C>G (p.Leu2609=)
NM_005045.4(RELN):c.78G>A (p.Ala26=) rs1196068638
NM_005045.4(RELN):c.8019C>T (p.Thr2673=) rs1329064994
NM_005045.4(RELN):c.8073T>C (p.Pro2691=) rs775986044

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