ClinVar Miner

List of variants in gene L1CAM reported as benign for not provided

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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_001278116.2(L1CAM):c.1268-114= rs5945359 0.99999
NM_001278116.2(L1CAM):c.2209-6C>T rs7885771 0.05725
NM_001278116.2(L1CAM):c.3458-34C>T rs7052999 0.05302
NM_001278116.2(L1CAM):c.3457+53C>T rs137915897 0.04426
NM_001278116.2(L1CAM):c.2431+147C>A rs4646266 0.04368
NM_001278116.2(L1CAM):c.1268-10C>T rs112841948 0.03467
NM_001278116.2(L1CAM):c.1939+98C>T rs55666951 0.03451
NM_001278116.2(L1CAM):c.855C>T (p.Ala285=) rs1042512 0.03189
NM_001278116.2(L1CAM):c.807-61G>C rs149290876 0.03149
NM_001278116.2(L1CAM):c.197+17G>A rs5987174 0.02545
NM_001278116.2(L1CAM):c.2307C>T (p.Ser769=) rs5987173 0.01697
NM_001278116.2(L1CAM):c.1704-14C>T rs140240430 0.01472
NM_001278116.2(L1CAM):c.2872C>G (p.Leu958Val) rs35902890 0.01086
NM_001278116.2(L1CAM):c.720G>A (p.Pro240=) rs35151382 0.01040
NM_001278116.2(L1CAM):c.28C>T (p.Pro10Ser) rs144605615 0.00970
NM_001278116.2(L1CAM):c.1977T>C (p.Pro659=) rs143382184 0.00854
NM_001278116.2(L1CAM):c.992-59G>A rs150150448 0.00534
NM_001278116.2(L1CAM):c.1002C>T (p.Tyr334=) rs73640833 0.00445
NM_001278116.2(L1CAM):c.992-32C>T rs191412165 0.00352
NM_001278116.2(L1CAM):c.3081G>A (p.Ala1027=) rs139393266 0.00285
NM_001278116.2(L1CAM):c.76+55C>T rs186040141 0.00201
NM_001278116.2(L1CAM):c.2302G>A (p.Val768Ile) rs36021462 0.00178
NM_001278116.2(L1CAM):c.396C>T (p.Ala132=) rs144708625 0.00131
NM_001278116.2(L1CAM):c.694+55G>A rs782068934 0.00091
NM_001278116.2(L1CAM):c.3543-22C>A rs199975913 0.00074
NM_001278116.2(L1CAM):c.1267+101G>A rs782529935 0.00057
NM_001278116.2(L1CAM):c.2432-86G>A rs782039832 0.00037
NM_001278116.2(L1CAM):c.2211G>A (p.Pro737=) rs146782397 0.00035
NM_001278116.2(L1CAM):c.113C>T (p.Thr38Met) rs201151358 0.00027
NM_001278116.2(L1CAM):c.294G>A (p.Thr98=) rs4898371 0.00014
NM_001278116.2(L1CAM):c.649A>C (p.Arg217=) rs201204893 0.00014
NM_001278116.2(L1CAM):c.1293G>A (p.Ala431=) rs137967792 0.00009
NM_001278116.2(L1CAM):c.1547-14C>T rs145192924 0.00009
NM_001278116.2(L1CAM):c.197+43A>G rs782420578 0.00004
NM_001278116.2(L1CAM):c.2763C>T (p.Pro921=) rs781813303 0.00001
NM_001278116.2(L1CAM):c.3543-11T>C rs782225211 0.00001
NM_001278116.2(L1CAM):c.92-180C>T rs976809372 0.00001
NM_001278116.2(L1CAM):c.*159T>C rs2148491713
NM_001278116.2(L1CAM):c.-31C>G rs2855584
NM_001278116.2(L1CAM):c.1704-18_1704-15del rs782806330
NM_001278116.2(L1CAM):c.2310C>T (p.Asp770=) rs2064717101
NM_001278116.2(L1CAM):c.2431+322dup rs374864697
NM_001278116.2(L1CAM):c.2431+336del rs374864697
NM_001278116.2(L1CAM):c.3323-84C>T rs2071127
NM_001278116.2(L1CAM):c.3457+116G>T rs782631703
NM_001278116.2(L1CAM):c.3457+18C>T rs76726076
NM_001278116.2(L1CAM):c.3458-139G>A rs56328570
NM_001278116.2(L1CAM):c.400+285G>A rs184593210
NM_001278116.2(L1CAM):c.401-89A>G rs12841858
NM_001278116.2(L1CAM):c.401-90T>G rs12834944
NM_001278116.2(L1CAM):c.523+45G>A rs192481307

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