ClinVar Miner

List of variants in gene LAMB2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_002292.4(LAMB2):c.109C>G (p.Pro37Ala) rs144765752 0.00242
NM_002292.4(LAMB2):c.3875A>T (p.Asn1292Ile) rs148246465 0.00175
NM_002292.4(LAMB2):c.4163G>A (p.Arg1388Gln) rs146522641 0.00159
NM_002292.4(LAMB2):c.1306G>A (p.Gly436Ser) rs142402808 0.00096
NM_002292.4(LAMB2):c.2975T>C (p.Ile992Thr) rs148732023 0.00086
NM_002292.4(LAMB2):c.4118A>G (p.Asp1373Gly) rs112933248 0.00076
NM_002292.4(LAMB2):c.703C>T (p.Arg235Trp) rs144133177 0.00071
NM_002292.4(LAMB2):c.2922G>C (p.Gly974=) rs145465720 0.00031
NM_002292.4(LAMB2):c.5142G>A (p.Lys1714=) rs139511264 0.00027
NM_002292.4(LAMB2):c.2322C>G (p.Thr774=) rs142116851 0.00026
NM_002292.4(LAMB2):c.5061G>A (p.Thr1687=) rs150465100 0.00025
NM_002292.4(LAMB2):c.101C>A (p.Ala34Asp) rs202057459 0.00024
NM_002292.4(LAMB2):c.4257T>C (p.Ala1419=) rs149536828 0.00016
NM_002292.4(LAMB2):c.4878G>A (p.Arg1626=) rs148648480 0.00016
NM_002292.4(LAMB2):c.2488+6C>G rs371384656 0.00012
NM_002292.4(LAMB2):c.1226-5G>A rs545564814 0.00006
NM_002292.4(LAMB2):c.1327C>T (p.His443Tyr) rs200732790 0.00006
NM_002292.4(LAMB2):c.1422A>C (p.Ala474=) rs201408584 0.00006
NM_002292.4(LAMB2):c.2099G>A (p.Gly700Glu) rs142860588 0.00006
NM_002292.4(LAMB2):c.2945G>A (p.Arg982Gln) rs149653966 0.00006
NM_002292.4(LAMB2):c.3498A>G (p.Pro1166=) rs186771094 0.00006
NM_002292.4(LAMB2):c.3641G>A (p.Arg1214Gln) rs202135107 0.00006
NM_002292.4(LAMB2):c.1891-11C>T rs778444207 0.00005
NM_002292.4(LAMB2):c.1572C>T (p.Cys524=) rs111883392 0.00004
NM_002292.4(LAMB2):c.2152C>T (p.Leu718=) rs756535650 0.00004
NM_002292.4(LAMB2):c.3797+4C>T rs368346725 0.00004
NM_002292.4(LAMB2):c.76+10C>T rs370554848 0.00003
NM_002292.4(LAMB2):c.3732C>T (p.Ile1244=) rs886038508 0.00002
NM_002292.4(LAMB2):c.1068C>T (p.Cys356=) rs751259636 0.00001
NM_002292.4(LAMB2):c.1291C>T (p.Leu431=) rs886038507 0.00001
NM_002292.4(LAMB2):c.2669C>T (p.Thr890Ile) rs527639885 0.00001
NM_002292.4(LAMB2):c.77-9T>C rs563352159 0.00001
NM_002292.4(LAMB2):c.1226-8G>C
NM_002292.4(LAMB2):c.1519-7C>T
NM_002292.4(LAMB2):c.1891-4C>A
NM_002292.4(LAMB2):c.2322C>T (p.Thr774=)
NM_002292.4(LAMB2):c.2766C>T (p.Gly922=)
NM_002292.4(LAMB2):c.3354C>T (p.Ala1118=)
NM_002292.4(LAMB2):c.4296T>C (p.Asp1432=)
NM_002292.4(LAMB2):c.4759C>T (p.Leu1587=)
NM_002292.4(LAMB2):c.726C>T (p.Ile242=)

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