ClinVar Miner

List of variants in gene LAMB1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 104
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HGVS dbSNP gnomAD frequency
NM_002291.3(LAMB1):c.1857+68A>C rs59832125 0.05405
NM_002291.3(LAMB1):c.1986-73G>C rs35953236 0.02899
NM_002291.3(LAMB1):c.3391+255G>T rs117582241 0.01874
NM_002291.3(LAMB1):c.2854+180T>C rs41281048 0.01826
NM_002291.3(LAMB1):c.1482+97C>A rs76897103 0.01758
NM_002291.3(LAMB1):c.423+174A>G rs74591776 0.01631
NM_002291.3(LAMB1):c.1857+57T>C rs115972989 0.01569
NM_002291.3(LAMB1):c.3946+257G>A rs77154077 0.01484
NM_002291.3(LAMB1):c.677-185C>T rs62468016 0.01355
NM_002291.3(LAMB1):c.3079+330A>G rs145386687 0.01299
NM_002291.3(LAMB1):c.1482+226A>T rs114782286 0.01293
NM_002291.3(LAMB1):c.37+145C>T rs147297312 0.01177
NC_000007.14:g.108003310T>C rs550839188 0.01126
NM_002291.3(LAMB1):c.2691-297C>T rs150990106 0.01101
NM_002291.3(LAMB1):c.3080-177G>A rs73420787 0.01083
NM_002291.3(LAMB1):c.37+56A>G rs139934214 0.01079
NM_002291.3(LAMB1):c.38-151C>T rs147357522 0.01077
NM_002291.3(LAMB1):c.2314+303C>T rs148674212 0.01076
NM_002291.3(LAMB1):c.3947-254A>G rs55810226 0.00947
NM_002291.3(LAMB1):c.*85A>G rs78245660 0.00941
NM_002291.3(LAMB1):c.3392-302A>T rs116052160 0.00933
NM_002291.3(LAMB1):c.1000+97T>A rs114359260 0.00872
NM_002291.3(LAMB1):c.3947-192C>T rs73725016 0.00651
NM_002291.3(LAMB1):c.1698+121T>C rs142874944 0.00584
NM_002291.3(LAMB1):c.3946+276C>T rs115829916 0.00550
NM_002291.3(LAMB1):c.1563-150del rs199783952 0.00522
NM_002291.3(LAMB1):c.4392+161dup rs377176589 0.00517
NM_002291.3(LAMB1):c.423+28T>C rs142134711 0.00501
NM_002291.3(LAMB1):c.2691-272A>C rs187514096 0.00494
NM_002291.3(LAMB1):c.3079+235A>G rs113339564 0.00490
NM_002291.3(LAMB1):c.1001-43A>G rs111506803 0.00476
NM_002291.3(LAMB1):c.3392-27C>T rs187768412 0.00446
NM_002291.3(LAMB1):c.1370-18C>T rs79590733 0.00436
NM_002291.3(LAMB1):c.214-136A>G rs147367343 0.00425
NM_002291.3(LAMB1):c.4392+34T>C rs114995359 0.00414
NM_002291.3(LAMB1):c.5064+107del rs376602413 0.00414
NM_002291.3(LAMB1):c.1001-219T>C rs147622101 0.00379
NM_002291.3(LAMB1):c.1482+146T>C rs143938527 0.00376
NM_002291.3(LAMB1):c.1482+129A>G rs146785096 0.00365
NM_002291.3(LAMB1):c.37+44A>G rs149826411 0.00359
NC_000007.14:g.108003301C>T rs375797805 0.00356
NM_002291.3(LAMB1):c.37+171G>A rs189826359 0.00356
NM_002291.3(LAMB1):c.2315-162G>A rs144019977 0.00355
NM_002291.3(LAMB1):c.1985+41T>A rs114714347 0.00340
NM_002291.3(LAMB1):c.213+270G>A rs144093284 0.00307
NM_002291.3(LAMB1):c.468T>C (p.Phe156=) rs149792171 0.00272
NM_002291.3(LAMB1):c.423+205G>T rs118073269 0.00271
NM_002291.3(LAMB1):c.2113G>C (p.Val705Leu) rs34150332 0.00242
NM_002291.3(LAMB1):c.476C>G (p.Thr159Ser) rs140146478 0.00233
NM_002291.3(LAMB1):c.677-32C>G rs188495767 0.00214
NM_002291.3(LAMB1):c.1590A>C (p.Ser530=) rs139481973 0.00175
NM_002291.3(LAMB1):c.1945G>A (p.Asp649Asn) rs142386151 0.00147
NM_002291.3(LAMB1):c.1189+11A>G rs111256901 0.00145
NM_002291.3(LAMB1):c.2557C>T (p.Arg853Trp) rs115746206 0.00141
NM_002291.3(LAMB1):c.1736G>A (p.Arg579Gln) rs115518856 0.00126
NM_002291.3(LAMB1):c.855A>G (p.Gly285=) rs140773514 0.00091
NM_002291.3(LAMB1):c.3594C>T (p.His1198=) rs566055806 0.00081
NM_002291.3(LAMB1):c.1483-14G>A rs115559402 0.00073
NM_002291.3(LAMB1):c.891C>T (p.His297=) rs146380871 0.00070
NM_002291.3(LAMB1):c.2277C>A (p.Ile759=) rs143597483 0.00054
NM_002291.3(LAMB1):c.3038G>A (p.Arg1013Gln) rs141390544 0.00054
NM_002291.3(LAMB1):c.3124G>A (p.Gly1042Ser) rs149204722 0.00043
NM_002291.3(LAMB1):c.1370-13T>G rs199712943 0.00041
NM_002291.3(LAMB1):c.1068C>T (p.Asn356=) rs34168368 0.00038
NM_002291.3(LAMB1):c.3946+44C>T rs78931465 0.00036
NM_002291.3(LAMB1):c.3135C>T (p.Cys1045=) rs145328837 0.00032
NM_002291.3(LAMB1):c.1482+19C>T rs376329632 0.00023
NM_002291.3(LAMB1):c.3642G>T (p.Gly1214=) rs569355700 0.00021
NM_002291.3(LAMB1):c.4947C>T (p.Ser1649=) rs190017087 0.00019
NM_002291.3(LAMB1):c.1074C>T (p.Ser358=) rs758179734 0.00011
NM_002291.3(LAMB1):c.349+19G>A rs756720953 0.00011
NM_002291.3(LAMB1):c.3079+42C>G rs563739071 0.00007
NM_002291.3(LAMB1):c.816C>T (p.Phe272=) rs562088411 0.00007
NM_002291.3(LAMB1):c.3498G>A (p.Thr1166=) rs778237047 0.00006
NM_002291.3(LAMB1):c.3444G>A (p.Thr1148=) rs753168303 0.00004
NM_002291.3(LAMB1):c.3639C>T (p.Ile1213=) rs141885441 0.00004
NM_002291.3(LAMB1):c.5325A>T (p.Ile1775=) rs369528849 0.00004
NM_002291.3(LAMB1):c.3762-4A>G rs374438596 0.00002
NM_002291.3(LAMB1):c.5268T>C (p.Asp1756=) rs149602697 0.00002
NM_002291.3(LAMB1):c.1603A>G (p.Met535Val) rs752556189 0.00001
NM_002291.3(LAMB1):c.1422C>G (p.Ser474=) rs780369106
NM_002291.3(LAMB1):c.1539C>T (p.Asp513=) rs1584519817
NM_002291.3(LAMB1):c.1563-277T>C rs114072767
NM_002291.3(LAMB1):c.1857+180dup rs57580761
NM_002291.3(LAMB1):c.1858-105G>C rs114250246
NM_002291.3(LAMB1):c.1977A>G (p.Pro659=) rs1057523829
NM_002291.3(LAMB1):c.1985+11C>G rs192349543
NM_002291.3(LAMB1):c.213+31G>A rs199884475
NM_002291.3(LAMB1):c.3300G>A (p.Thr1100=) rs139955747
NM_002291.3(LAMB1):c.3392-220_3392-219del rs373001222
NM_002291.3(LAMB1):c.3510G>A (p.Ser1170=) rs373235081
NM_002291.3(LAMB1):c.38-164C>T rs139532877
NM_002291.3(LAMB1):c.38-28C>A rs112819389
NM_002291.3(LAMB1):c.3946+16T>C rs777888220
NM_002291.3(LAMB1):c.4074C>T (p.Asp1358=) rs146681738
NM_002291.3(LAMB1):c.4188+62A>C rs199891469
NM_002291.3(LAMB1):c.5064+282_5064+284del rs34631145
NM_002291.3(LAMB1):c.5225-22AT[4] rs113854298
NM_002291.3(LAMB1):c.5225-22AT[8] rs113854298
NM_002291.3(LAMB1):c.5225-9_5225-8insTA rs142305198
NM_002291.3(LAMB1):c.880-291_880-289del rs11350102
NM_002291.3(LAMB1):c.880-305dup rs11350102
NM_002291.3(LAMB1):c.880-307_880-303del rs200315734
NM_002291.3(LAMB1):c.981A>T (p.Arg327=) rs1554410490

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