ClinVar Miner

List of variants in gene LAMA2 reported as likely benign for not specified

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Gene type:
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Total variants: 126
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HGVS dbSNP gnomAD frequency
NM_000426.4(LAMA2):c.3412G>A (p.Val1138Met) rs2306942 0.09135
NM_000426.4(LAMA2):c.8028T>C (p.Asn2676=) rs35313209 0.02285
NM_000426.4(LAMA2):c.8528A>G (p.Asn2843Ser) rs73599293 0.02196
NM_000426.4(LAMA2):c.1467+38C>T rs78299321 0.02120
NM_000426.4(LAMA2):c.1533T>C (p.Asn511=) rs9492266 0.02106
NM_000426.4(LAMA2):c.4750G>A (p.Gly1584Ser) rs117781224 0.01941
NM_000426.4(LAMA2):c.1491T>C (p.Cys497=) rs2306220 0.01733
NM_000426.4(LAMA2):c.8124T>A (p.Gly2708=) rs34997144 0.01727
NM_000426.4(LAMA2):c.8691A>G (p.Arg2897=) rs2228599 0.01648
NM_000426.4(LAMA2):c.3613A>G (p.Thr1205Ala) rs35889149 0.01262
NM_000426.4(LAMA2):c.1798G>A (p.Gly600Arg) rs36044314 0.01250
NM_000426.4(LAMA2):c.2857-39T>C rs117096733 0.01035
NM_000426.4(LAMA2):c.1206+11C>T rs115007959 0.00915
NM_000426.4(LAMA2):c.7431A>T (p.Arg2477Ser) rs34367843 0.00914
NM_000426.4(LAMA2):c.1930C>G (p.His644Asp) rs35879899 0.00899
NM_000426.4(LAMA2):c.5727-27C>A rs116128872 0.00884
NM_000426.4(LAMA2):c.8548-10T>C rs113644365 0.00865
NM_000426.4(LAMA2):c.9123C>T (p.Val3041=) rs61749497 0.00858
NM_000426.4(LAMA2):c.1884+50A>C rs116773503 0.00785
NM_000426.4(LAMA2):c.2476C>T (p.Arg826Trp) rs118147866 0.00549
NM_000426.4(LAMA2):c.3556-15T>G rs17741922 0.00414
NM_000426.4(LAMA2):c.4718-37G>A rs115237621 0.00359
NM_000426.4(LAMA2):c.4487C>T (p.Ala1496Val) rs147077184 0.00338
NM_000426.4(LAMA2):c.4935C>A (p.Thr1645=) rs35579821 0.00306
NM_000426.4(LAMA2):c.6788C>T (p.Thr2263Met) rs56209257 0.00301
NM_000426.4(LAMA2):c.6429+8C>A rs199773264 0.00238
NM_000426.4(LAMA2):c.411G>A (p.Ala137=) rs149347601 0.00206
NM_000426.4(LAMA2):c.2462C>T (p.Thr821Met) rs117422805 0.00173
NM_000426.4(LAMA2):c.1308T>G (p.Gly436=) rs41285286 0.00165
NM_000426.4(LAMA2):c.1782+14T>C rs191215452 0.00147
NM_000426.4(LAMA2):c.2323-19A>T rs139093294 0.00128
NM_000426.4(LAMA2):c.2856+13G>A rs149487202 0.00121
NM_000426.4(LAMA2):c.255C>T (p.Ile85=) rs142083777 0.00116
NM_000426.4(LAMA2):c.1814C>T (p.Thr605Ile) rs112388307 0.00103
NM_000426.4(LAMA2):c.397-15G>A rs188045427 0.00098
NM_000426.4(LAMA2):c.6649G>A (p.Val2217Ile) rs147857398 0.00093
NM_000426.4(LAMA2):c.909+32T>A rs374692035 0.00091
NM_000426.4(LAMA2):c.9211+6T>C rs201375881 0.00091
NM_000426.4(LAMA2):c.4311+32C>G rs148912474 0.00090
NM_000426.4(LAMA2):c.922G>A (p.Glu308Lys) rs146462599 0.00086
NM_000426.4(LAMA2):c.2323-18T>A rs199846930 0.00081
NM_000426.4(LAMA2):c.2187G>C (p.Gly729=) rs142345851 0.00077
NM_000426.4(LAMA2):c.8586T>C (p.Tyr2862=) rs142451929 0.00074
NM_000426.4(LAMA2):c.2115T>G (p.Leu705=) rs149753273 0.00065
NM_000426.4(LAMA2):c.5121C>T (p.Asp1707=) rs151199929 0.00064
NM_000426.4(LAMA2):c.6085+17C>T rs185719358 0.00063
NM_000426.4(LAMA2):c.7300+10T>A rs200469923 0.00056
NM_000426.4(LAMA2):c.4176+9C>T rs117116822 0.00042
NM_000426.4(LAMA2):c.2217G>T (p.Trp739Cys) rs192317605 0.00039
NM_000426.4(LAMA2):c.2857-13C>T rs201188972 0.00037
NM_000426.4(LAMA2):c.7300+19A>G rs115892449 0.00036
NM_000426.4(LAMA2):c.4740C>A (p.Gly1580=) rs371629354 0.00034
NM_000426.4(LAMA2):c.9211+17C>T rs367830612 0.00021
NM_000426.4(LAMA2):c.2304C>T (p.Asp768=) rs142126511 0.00020
NM_000426.4(LAMA2):c.2766C>T (p.Ala922=) rs149254699 0.00019
NM_000426.4(LAMA2):c.8989-12C>G rs144860334 0.00017
NM_000426.4(LAMA2):c.408C>T (p.Ile136=) rs145149634 0.00016
NM_000426.4(LAMA2):c.7395T>C (p.Asp2465=) rs140483001 0.00014
NM_000426.4(LAMA2):c.8076-15A>G rs368086451 0.00013
NM_000426.4(LAMA2):c.3597T>C (p.Asp1199=) rs199904029 0.00011
NM_000426.4(LAMA2):c.5769A>G (p.Ala1923=) rs200582139 0.00011
NM_000426.4(LAMA2):c.6666G>A (p.Leu2222=) rs772358536 0.00011
NM_000426.4(LAMA2):c.8244+13A>G rs1057523272 0.00011
NM_000426.4(LAMA2):c.8907C>T (p.Arg2969=) rs367622610 0.00011
NM_000426.4(LAMA2):c.1207-28G>A rs112735359 0.00010
NM_000426.4(LAMA2):c.2736G>A (p.Ala912=) rs142671449 0.00009
NM_000426.4(LAMA2):c.5317C>T (p.Arg1773Trp) rs138695453 0.00009
NM_000426.4(LAMA2):c.8223G>A (p.Thr2741=) rs150596964 0.00009
NM_000426.4(LAMA2):c.1468-19T>C rs200241408 0.00008
NM_000426.4(LAMA2):c.6345C>T (p.Pro2115=) rs200364660 0.00008
NM_000426.4(LAMA2):c.7452-9A>G rs748647936 0.00008
NM_000426.4(LAMA2):c.711C>T (p.Ser237=) rs369745832 0.00007
NM_000426.4(LAMA2):c.4059-20T>C rs764866830 0.00006
NM_000426.4(LAMA2):c.4157A>T (p.Tyr1386Phe) rs560139751 0.00006
NM_000426.4(LAMA2):c.5969-6T>C rs201913996 0.00006
NM_000426.4(LAMA2):c.8637G>C (p.Leu2879=) rs370496870 0.00006
NM_000426.4(LAMA2):c.5454G>A (p.Lys1818=) rs759312395 0.00005
NM_000426.4(LAMA2):c.5969-4G>A rs566302197 0.00005
NM_000426.4(LAMA2):c.5280G>A (p.Glu1760=) rs376693904 0.00004
NM_000426.4(LAMA2):c.5469C>T (p.Ser1823=) rs753886576 0.00004
NM_000426.4(LAMA2):c.8075+16C>T rs776913896 0.00004
NM_000426.4(LAMA2):c.5382A>G (p.Thr1794=) rs565429072 0.00003
NM_000426.4(LAMA2):c.6702A>T (p.Ala2234=) rs372212378 0.00003
NM_000426.4(LAMA2):c.7479C>T (p.Ser2493=) rs368989339 0.00003
NM_000426.4(LAMA2):c.4456G>A (p.Ala1486Thr) rs372576669 0.00002
NM_000426.4(LAMA2):c.6430-18A>G rs1424400019 0.00002
NM_000426.4(LAMA2):c.2265G>A (p.Glu755=) rs910253334 0.00001
NM_000426.4(LAMA2):c.2376C>T (p.Phe792=) rs150046431 0.00001
NM_000426.4(LAMA2):c.2537+12C>T rs376097319 0.00001
NM_000426.4(LAMA2):c.2749+24C>A rs886038292 0.00001
NM_000426.4(LAMA2):c.3175-19G>C rs184243762 0.00001
NM_000426.4(LAMA2):c.3175-22G>A rs777129293 0.00001
NM_000426.4(LAMA2):c.4296A>G (p.Glu1432=) rs1423553661 0.00001
NM_000426.4(LAMA2):c.4857A>G (p.Leu1619=) rs777158791 0.00001
NM_000426.4(LAMA2):c.7451+37A>G rs886038294 0.00001
NM_000426.4(LAMA2):c.7573-9T>C rs369082375 0.00001
NM_000426.4(LAMA2):c.7680C>T (p.Ser2560=) rs750957928 0.00001
NM_000426.4(LAMA2):c.8937G>C (p.Gly2979=) rs1194078171 0.00001
NM_000426.4(LAMA2):c.-17del rs537351244
NM_000426.4(LAMA2):c.113-14T>A rs1311979480
NM_000426.4(LAMA2):c.2430A>G (p.Pro810=) rs147572139
NM_000426.4(LAMA2):c.2450+16A>G rs1024374408
NM_000426.4(LAMA2):c.2451-18G>A rs142989915
NM_000426.4(LAMA2):c.2756G>T (p.Arg919Leu) rs35277491
NM_000426.4(LAMA2):c.2857-14T>A rs535718824
NM_000426.4(LAMA2):c.3296A>G (p.Asn1099Ser) rs35065563
NM_000426.4(LAMA2):c.3925-6T>A rs372612467
NM_000426.4(LAMA2):c.3969T>C (p.Thr1323=) rs112327654
NM_000426.4(LAMA2):c.4436+6A>G rs1057523624
NM_000426.4(LAMA2):c.4656C>A (p.Ala1552=) rs1057524318
NM_000426.4(LAMA2):c.4717+12_4717+20dup rs761353189
NM_000426.4(LAMA2):c.5234+19A>G rs1554287019
NM_000426.4(LAMA2):c.5235-8G>A rs1554287355
NM_000426.4(LAMA2):c.5448A>G (p.Lys1816=) rs1554289590
NM_000426.4(LAMA2):c.5530C>A (p.Arg1844Ser) rs56173620
NM_000426.4(LAMA2):c.5866-15T>C rs774886204
NM_000426.4(LAMA2):c.6706A>C (p.Arg2236=) rs886038293
NM_000426.4(LAMA2):c.7473A>G (p.Lys2491=) rs886038295
NM_000426.4(LAMA2):c.7536C>T (p.Pro2512=) rs778297793
NM_000426.4(LAMA2):c.8076-24A>G rs886038296
NM_000426.4(LAMA2):c.9039T>C (p.Asp3013=) rs1057523899
NM_000426.4(LAMA2):c.9051A>G (p.Pro3017=) rs1057522162
NM_000426.4(LAMA2):c.910-14del rs769173629
NM_000426.4(LAMA2):c.9211+21C>A rs886038297
NM_000426.4(LAMA2):c.9339C>A (p.Gly3113=) rs182391310
NM_000426.4(LAMA2):c.99A>G (p.Ala33=) rs762858697

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