ClinVar Miner

List of variants in gene LAMB3 reported as benign for not provided

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Gene type:
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Total variants: 89
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HGVS dbSNP gnomAD frequency
NM_000228.3(LAMB3):c.2702-12dup rs397807887 0.95488
NM_000228.3(LAMB3):c.-37-381T>A rs10779510 0.87193
NM_000228.3(LAMB3):c.823-15C>T rs4844863 0.84219
NM_000228.3(LAMB3):c.1716T>C (p.Cys572=) rs2179402 0.74805
NM_000228.3(LAMB3):c.184-70A>G rs2076357 0.57810
NM_000228.3(LAMB3):c.291A>C (p.Ser97=) rs2076356 0.56410
NM_000228.3(LAMB3):c.3432A>G (p.Ser1144=) rs1049607 0.44327
NM_000228.3(LAMB3):c.2909+182C>T rs2076221 0.35189
NM_000228.3(LAMB3):c.3383-334C>T rs2076227 0.33839
NM_000228.3(LAMB3):c.384C>T (p.Pro128=) rs1130667 0.30741
NM_000228.3(LAMB3):c.1976+169T>C rs4844860 0.29396
NM_000228.3(LAMB3):c.2910-169G>A rs2076220 0.29074
NM_000228.3(LAMB3):c.1976+222C>T rs9430008 0.28860
NM_000228.3(LAMB3):c.298+50T>A rs2076355 0.28812
NM_000228.3(LAMB3):c.2556+60C>T rs3737913 0.27290
NM_000228.3(LAMB3):c.*102C>T rs2566 0.27226
NM_000228.3(LAMB3):c.138C>T (p.Thr46=) rs2228339 0.25110
NM_000228.3(LAMB3):c.28+292G>A rs2076359 0.25084
NM_000228.3(LAMB3):c.-37-573C>T rs3753522 0.25081
NM_000228.3(LAMB3):c.28+326C>T rs2076358 0.25077
NM_000228.3(LAMB3):c.564+286C>T rs12137442 0.16127
NM_000228.3(LAMB3):c.-37-500C>T rs3753523 0.15286
NM_000228.3(LAMB3):c.1133-172A>G rs2076353 0.13166
NM_000228.3(LAMB3):c.1579G>A (p.Val527Met) rs2076349 0.12644
NM_000228.3(LAMB3):c.1486-18G>A rs2076350 0.12625
NM_000228.3(LAMB3):c.1289-52G>A rs2072938 0.12083
NM_000228.3(LAMB3):c.184-286A>G rs10127604 0.11453
NM_000228.3(LAMB3):c.2673A>G (p.Leu891=) rs3179860 0.11219
NM_000228.3(LAMB3):c.2554A>T (p.Met852Leu) rs12748250 0.11215
NM_000228.3(LAMB3):c.1132+124G>A rs12567766 0.08521
NM_000228.3(LAMB3):c.1149G>A (p.Pro383=) rs2076351 0.05772
NM_000228.3(LAMB3):c.943+52C>G rs34311919 0.05174
NM_000228.3(LAMB3):c.1312T>A (p.Ser438Thr) rs2229468 0.04067
NM_000228.3(LAMB3):c.3448C>T (p.Leu1150=) rs2228342 0.03922
NM_000228.3(LAMB3):c.1288+29G>A rs75181751 0.03477
NM_000228.3(LAMB3):c.564+250C>T rs75509432 0.03211
NM_000228.3(LAMB3):c.2702-14G>A rs199838217 0.02820
NM_000228.3(LAMB3):c.822+296A>T rs963436 0.02764
NM_000228.3(LAMB3):c.1764T>C (p.Tyr588=) rs2229465 0.02743
NM_000228.3(LAMB3):c.943+18C>A rs7550377 0.02735
NM_000228.3(LAMB3):c.2777C>A (p.Ala926Asp) rs2076222 0.02691
NM_000228.3(LAMB3):c.2910-115C>T rs2076219 0.02684
NM_000228.3(LAMB3):c.2124T>C (p.Ser708=) rs2072937 0.02665
NM_000228.3(LAMB3):c.1133-34T>C rs2076352 0.02654
NM_000228.3(LAMB3):c.2069A>G (p.Asn690Ser) rs2229466 0.02614
NM_000228.3(LAMB3):c.541A>G (p.Asn181Asp) rs2235542 0.02610
NM_000228.3(LAMB3):c.564+10G>A rs12410975 0.02306
NM_000228.3(LAMB3):c.28+88G>A rs58281786 0.01925
NM_000228.3(LAMB3):c.1289-150C>T rs113875858 0.01908
NM_000228.3(LAMB3):c.2723C>T (p.Thr908Ile) rs61753424 0.01891
NM_000228.3(LAMB3):c.3383-58G>A rs77567304 0.01856
NM_000228.3(LAMB3):c.2556+13G>A rs113339950 0.01851
NM_000228.3(LAMB3):c.2909+194C>T rs6674461 0.01728
NM_000228.3(LAMB3):c.2542C>T (p.Arg848Trp) rs59260335 0.01279
NM_000228.3(LAMB3):c.1015T>C (p.Tyr339His) rs52814161 0.01066
NM_000228.3(LAMB3):c.2260C>T (p.Arg754Trp) rs62637710 0.00948
NM_000228.3(LAMB3):c.689G>C (p.Arg230Thr) rs61734502 0.00697
NM_000228.3(LAMB3):c.1439C>T (p.Pro480Leu) rs61734494 0.00363
NM_000228.3(LAMB3):c.372+10C>T rs192386323 0.00302
NM_000228.3(LAMB3):c.2286C>T (p.Thr762=) rs11555726 0.00282
NM_000228.3(LAMB3):c.867T>C (p.Asn289=) rs115579649 0.00254
NM_000228.3(LAMB3):c.332A>G (p.Asp111Gly) rs55824996 0.00198
NM_000228.3(LAMB3):c.15C>T (p.Phe5=) rs140470350 0.00190
NM_000228.3(LAMB3):c.-37-26A>T rs145315604 0.00153
NM_000228.3(LAMB3):c.2076C>T (p.Leu692=) rs140248040 0.00139
NM_000228.3(LAMB3):c.2359-15G>A rs147708427 0.00111
NM_000228.3(LAMB3):c.1194G>A (p.Gln398=) rs116602483 0.00103
NM_000228.3(LAMB3):c.1413G>A (p.Lys471=) rs112316651 0.00096
NM_000228.3(LAMB3):c.1188C>T (p.Thr396=) rs115883756 0.00082
NM_000228.3(LAMB3):c.2702-9dup rs775872328 0.00056
NM_000228.3(LAMB3):c.2403C>T (p.Cys801=) rs115279528 0.00017
NM_000228.3(LAMB3):c.3479A>G (p.His1160Arg) rs147931502 0.00016
NM_000228.3(LAMB3):c.1008G>A (p.Gln336=) rs114404740 0.00008
NM_000228.3(LAMB3):c.1236A>G (p.Leu412=) rs202113091 0.00003
NM_000228.3(LAMB3):c.3252G>A (p.Lys1084=) rs372120856 0.00003
NM_000228.3(LAMB3):c.1289-186G>A rs61822212
NM_000228.3(LAMB3):c.184-335C>T rs9430010
NM_000228.3(LAMB3):c.184-335del rs10712661
NM_000228.3(LAMB3):c.2138-20C>T
NM_000228.3(LAMB3):c.2605C>A (p.Arg869Ser) rs11555728
NM_000228.3(LAMB3):c.2702-12G>A
NM_000228.3(LAMB3):c.2777C>G (p.Ala926Gly) rs2076222
NM_000228.3(LAMB3):c.28+163C>G rs2076360
NM_000228.3(LAMB3):c.372+16dup
NM_000228.3(LAMB3):c.373-15C>T rs377371473
NM_000228.3(LAMB3):c.781C>G (p.Pro261Ala)
NM_000228.3(LAMB3):c.822+33G>C rs2072940
NM_000228.3(LAMB3):c.823-7del
NM_000228.3(LAMB3):c.943+18_943+19insA

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