ClinVar Miner

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

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Gene type:
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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_001364905.1(LRBA):c.1756-140G>A rs1148648 0.95669
NM_001364905.1(LRBA):c.1360-40A>G rs1201207 0.95627
NM_001364905.1(LRBA):c.1755+202T>G rs1201213 0.95545
NM_001364905.1(LRBA):c.6551+84A>G rs7674989 0.87341
NM_001364905.1(LRBA):c.5646-71G>A rs1993109 0.69833
NM_001364905.1(LRBA):c.646-264T>G rs10031124 0.69504
NM_001364905.1(LRBA):c.1756-207G>T rs1365380 0.69138
NM_001364905.1(LRBA):c.7849+10A>G rs1813134 0.62993
NM_001364905.1(LRBA):c.7363-244G>T rs2292207 0.61439
NM_001364905.1(LRBA):c.7195-141T>C rs13145548 0.61210
NM_001364905.1(LRBA):c.8468+182A>T rs1870515 0.56114
NM_001364905.1(LRBA):c.6552-202C>G rs7673944 0.39975
NM_001364905.1(LRBA):c.1015-159A>G rs13150306 0.26274
NM_001364905.1(LRBA):c.4730-301C>A rs11736357 0.25361
NM_001364905.1(LRBA):c.7363-186G>A rs1507191 0.24858
NM_001364905.1(LRBA):c.6921+60C>G rs2292122 0.21963
NM_001364905.1(LRBA):c.6922-40C>A rs2271043 0.21960
NM_001364905.1(LRBA):c.6921+278C>G rs62348580 0.21948
NM_001364905.1(LRBA):c.2368-284A>T rs57003564 0.21947
NM_001364905.1(LRBA):c.6668-241C>T rs72734475 0.21704
NM_001364905.1(LRBA):c.6331-159A>G rs55998463 0.21669
NM_001364905.1(LRBA):c.8077G>A (p.Ala2693Thr) rs3749574 0.21105
NM_001364905.1(LRBA):c.8393C>T (p.Ser2798Leu) rs2290846 0.18590
NM_001364905.1(LRBA):c.7630+31G>A rs11737450 0.17416
NM_001364905.1(LRBA):c.5550T>C (p.Val1850=) rs1129998 0.17226
NM_001364905.1(LRBA):c.7194+308C>T rs76325768 0.14937
NM_001364905.1(LRBA):c.6667+257A>T rs17589134 0.14646
NM_001364905.1(LRBA):c.3269C>G (p.Ala1090Gly) rs1782360 0.12249
NM_001364905.1(LRBA):c.4730-303A>C rs1618979 0.12093
NM_001364905.1(LRBA):c.1347A>G (p.Ala449=) rs1201208 0.10667
NM_001364905.1(LRBA):c.-220+150T>C rs7665453 0.09854
NM_001364905.1(LRBA):c.-219-136G>A rs7665597 0.09773
NM_001364905.1(LRBA):c.5518+203C>T rs17027116 0.09320
NM_001364905.1(LRBA):c.5645+167T>A rs13340305 0.09220
NM_001364905.1(LRBA):c.2258+173T>A rs62344571 0.08803
NM_001364905.1(LRBA):c.8468+132G>A rs56145629 0.08602
NM_001364905.1(LRBA):c.1756-238T>A rs7655512 0.07113
NM_001364905.1(LRBA):c.2367+96A>C rs41280457 0.06171
NM_001364905.1(LRBA):c.6922-274G>A rs13130993 0.05584
NM_001364905.1(LRBA):c.646-154C>T rs36089213 0.05430
NM_001364905.1(LRBA):c.7693+215G>A rs76927516 0.04908
NM_001364905.1(LRBA):c.7194+251_7194+254dup rs144548467 0.03634
NM_001364905.1(LRBA):c.7694-292T>C rs80256015 0.03217
NM_001364905.1(LRBA):c.6781-3C>T rs58873298 0.02593
NM_001364905.1(LRBA):c.2674G>A (p.Ala892Thr) rs151098394 0.00465
NM_001364905.1(LRBA):c.8328G>A (p.Leu2776=) rs116828023 0.00357
NM_001364905.1(LRBA):c.5030A>G (p.Asn1677Ser) rs17027133 0.00349
GRCh37/hg19 4q31.3(chr4:151356081-151454015)x3
GRCh37/hg19 4q31.3(chr4:151880765-151901433)x1
NM_001364905.1(LRBA):c.1144T>C (p.Leu382=) rs62344598
NM_001364905.1(LRBA):c.1161+101del rs372369181
NM_001364905.1(LRBA):c.217-21dup rs766044503
NM_001364905.1(LRBA):c.217-307A>C rs2407548
NM_001364905.1(LRBA):c.4339+253_4339+255del rs9331496
NM_001364905.1(LRBA):c.4339+255del rs9331496
NM_001364905.1(LRBA):c.4730-299_4730-298del rs34994399
NM_001364905.1(LRBA):c.4730-301_4730-300insA rs770518067
NM_001364905.1(LRBA):c.4730-302_4730-301insA rs1560878315
NM_001364905.1(LRBA):c.550-108C>G rs58328072
NM_001364905.1(LRBA):c.5518+249_5518+250del rs10566622
NM_001364905.1(LRBA):c.5518+250del rs10566622
NM_001364905.1(LRBA):c.6193+150A>C rs4401437
NM_001364905.1(LRBA):c.6551+130_6551+131del rs77312120
NM_001364905.1(LRBA):c.7693+25C>T rs78877620
NM_001364905.1(LRBA):c.7850-306G>A rs11728745
NM_001364905.1(LRBA):c.8469-52_8469-48dup rs150278643

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