ClinVar Miner

List of variants in gene LAMA2 reported as likely benign by GeneDx

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Gene type:
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Total variants: 130
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HGVS dbSNP
NM_000426.3(LAMA2):c.-17del rs537351244
NM_000426.3(LAMA2):c.113-14T>A rs1311979480
NM_000426.3(LAMA2):c.1207-134G>A
NM_000426.3(LAMA2):c.1308T>G (p.Gly436=) rs41285286
NM_000426.3(LAMA2):c.1468-19T>C rs200241408
NM_000426.3(LAMA2):c.1468-268C>T
NM_000426.3(LAMA2):c.1621A>G (p.Ser541Gly) rs141363186
NM_000426.3(LAMA2):c.1782+10C>T rs200030296
NM_000426.3(LAMA2):c.1782+14T>C rs191215452
NM_000426.3(LAMA2):c.1814C>T (p.Thr605Ile) rs112388307
NM_000426.3(LAMA2):c.1884+115A>T
NM_000426.3(LAMA2):c.1885-19C>A rs372219177
NM_000426.3(LAMA2):c.2115T>G (p.Leu705=) rs149753273
NM_000426.3(LAMA2):c.2187G>C (p.Gly729=) rs142345851
NM_000426.3(LAMA2):c.2208+112G>T
NM_000426.3(LAMA2):c.2265G>A (p.Glu755=) rs910253334
NM_000426.3(LAMA2):c.2304C>T (p.Asp768=) rs142126511
NM_000426.3(LAMA2):c.2323-18T>A rs199846930
NM_000426.3(LAMA2):c.2323-19A>T rs139093294
NM_000426.3(LAMA2):c.2430A>C (p.Pro810=) rs147572139
NM_000426.3(LAMA2):c.2430A>G (p.Pro810=) rs147572139
NM_000426.3(LAMA2):c.2450+16A>G rs1024374408
NM_000426.3(LAMA2):c.2450+283A>G
NM_000426.3(LAMA2):c.2451-189C>T
NM_000426.3(LAMA2):c.2451-18G>A rs142989915
NM_000426.3(LAMA2):c.2537+12C>T rs376097319
NM_000426.3(LAMA2):c.255C>T (p.Ile85=) rs142083777
NM_000426.3(LAMA2):c.2755C>T (p.Arg919Cys) rs138018456
NM_000426.3(LAMA2):c.2766C>T (p.Ala922=) rs149254699
NM_000426.3(LAMA2):c.2856+13G>A rs149487202
NM_000426.3(LAMA2):c.2857-13C>T rs201188972
NM_000426.3(LAMA2):c.3175-19G>C rs184243762
NM_000426.3(LAMA2):c.3429C>A (p.Ile1143=) rs200646230
NM_000426.3(LAMA2):c.3582T>C (p.Ile1194=) rs137962409
NM_000426.3(LAMA2):c.3597T>C (p.Asp1199=) rs199904029
NM_000426.3(LAMA2):c.3615G>A (p.Thr1205=) rs374656305
NM_000426.3(LAMA2):c.397-15G>A rs188045427
NM_000426.3(LAMA2):c.397-23TTG[2] rs748624866
NM_000426.3(LAMA2):c.4059-20T>C rs764866830
NM_000426.3(LAMA2):c.408C>T (p.Ile136=) rs145149634
NM_000426.3(LAMA2):c.411G>A (p.Ala137=) rs149347601
NM_000426.3(LAMA2):c.4176+9C>T rs117116822
NM_000426.3(LAMA2):c.4177-73C>T
NM_000426.3(LAMA2):c.4296A>G (p.Glu1432=) rs1423553661
NM_000426.3(LAMA2):c.4436+6A>G rs1057523624
NM_000426.3(LAMA2):c.4487C>T (p.Ala1496Val) rs147077184
NM_000426.3(LAMA2):c.4656C>A (p.Ala1552=) rs1057524318
NM_000426.3(LAMA2):c.4717+12_4717+20dup rs761353189
NM_000426.3(LAMA2):c.4740C>A (p.Gly1580=) rs371629354
NM_000426.3(LAMA2):c.4857A>G (p.Leu1619=) rs777158791
NM_000426.3(LAMA2):c.4926A>G (p.Thr1642=) rs62421010
NM_000426.3(LAMA2):c.4935C>A (p.Thr1645=) rs35579821
NM_000426.3(LAMA2):c.4959+6G>T rs148060790
NM_000426.3(LAMA2):c.4960-16G>A rs9483026
NM_000426.3(LAMA2):c.5234+19A>G rs1554287019
NM_000426.3(LAMA2):c.5235-8G>A rs1554287355
NM_000426.3(LAMA2):c.5247C>T (p.Ala1749=) rs149951387
NM_000426.3(LAMA2):c.5317C>T (p.Arg1773Trp) rs138695453
NM_000426.3(LAMA2):c.5448A>G (p.Lys1816=) rs1554289590
NM_000426.3(LAMA2):c.5454G>A (p.Lys1818=) rs759312395
NM_000426.3(LAMA2):c.5469C>T (p.Ser1823=) rs753886576
NM_000426.3(LAMA2):c.5530C>A (p.Arg1844Ser) rs56173620
NM_000426.3(LAMA2):c.5563-161C>T
NM_000426.3(LAMA2):c.5633C>T (p.Ser1878Phe) rs139586720
NM_000426.3(LAMA2):c.5688C>T (p.His1896=) rs573779258
NM_000426.3(LAMA2):c.5726+39T>C
NM_000426.3(LAMA2):c.5866-15T>C rs774886204
NM_000426.3(LAMA2):c.5969-4G>A rs566302197
NM_000426.3(LAMA2):c.5969-5C>T rs201853235
NM_000426.3(LAMA2):c.5969-6T>C rs201913996
NM_000426.3(LAMA2):c.6085+17C>T rs185719358
NM_000426.3(LAMA2):c.6086-16C>T
NM_000426.3(LAMA2):c.6086-4A>G
NM_000426.3(LAMA2):c.6150T>C (p.Asp2050=) rs114766691
NM_000426.3(LAMA2):c.6161A>G (p.Gln2054Arg) rs56035053
NM_000426.3(LAMA2):c.6269-282G>A
NM_000426.3(LAMA2):c.6279C>T (p.Ala2093=) rs141190803
NM_000426.3(LAMA2):c.6339C>T (p.Leu2113=) rs752356162
NM_000426.3(LAMA2):c.6345C>T (p.Pro2115=) rs200364660
NM_000426.3(LAMA2):c.6429+8C>A rs199773264
NM_000426.3(LAMA2):c.6430-18A>G rs1424400019
NM_000426.3(LAMA2):c.6430-5dup rs550488535
NM_000426.3(LAMA2):c.6649G>A (p.Val2217Ile) rs147857398
NM_000426.3(LAMA2):c.6666G>A (p.Leu2222=) rs772358536
NM_000426.3(LAMA2):c.6697G>A (p.Val2233Ile) rs150945378
NM_000426.3(LAMA2):c.6707+314T>C
NM_000426.3(LAMA2):c.6708-201T>A
NM_000426.3(LAMA2):c.675C>T (p.Ala225=) rs139665175
NM_000426.3(LAMA2):c.6788C>T (p.Thr2263Met) rs56209257
NM_000426.3(LAMA2):c.7058G>A (p.Arg2353His) rs548483084
NM_000426.3(LAMA2):c.711C>T (p.Ser237=) rs369745832
NM_000426.3(LAMA2):c.7300+10T>A rs200469923
NM_000426.3(LAMA2):c.7300+19A>G rs115892449
NM_000426.3(LAMA2):c.7440-9G>A rs369558532
NM_000426.3(LAMA2):c.7452-9A>G rs748647936
NM_000426.3(LAMA2):c.7479C>T (p.Ser2493=) rs368989339
NM_000426.3(LAMA2):c.74C>T (p.Pro25Leu) rs145310035
NM_000426.3(LAMA2):c.7536C>T (p.Pro2512=) rs778297793
NM_000426.3(LAMA2):c.7640G>A (p.Gly2547Glu) rs115488979
NM_000426.3(LAMA2):c.7680C>T (p.Ser2560=) rs750957928
NM_000426.3(LAMA2):c.7898+131C>T
NM_000426.3(LAMA2):c.8075+16C>T rs776913896
NM_000426.3(LAMA2):c.8076-15A>G rs368086451
NM_000426.3(LAMA2):c.8223G>A (p.Thr2741=) rs150596964
NM_000426.3(LAMA2):c.8244+13A>G rs1057523272
NM_000426.3(LAMA2):c.8245-167G>A
NM_000426.3(LAMA2):c.8245-172G>T
NM_000426.3(LAMA2):c.8357+117T>C
NM_000426.3(LAMA2):c.8357+19C>T rs1057523035
NM_000426.3(LAMA2):c.8358-76C>T
NM_000426.3(LAMA2):c.8547+241T>C
NM_000426.3(LAMA2):c.8548-288T>C
NM_000426.3(LAMA2):c.8586T>C (p.Tyr2862=) rs142451929
NM_000426.3(LAMA2):c.8637G>C (p.Leu2879=) rs370496870
NM_000426.3(LAMA2):c.8703+314T>C
NM_000426.3(LAMA2):c.8727C>T (p.Cys2909=) rs148285711
NM_000426.3(LAMA2):c.8755C>T (p.Pro2919Ser) rs143026295
NM_000426.3(LAMA2):c.8858-229A>G
NM_000426.3(LAMA2):c.8937G>C (p.Gly2979=) rs1194078171
NM_000426.3(LAMA2):c.8988+15T>C rs201041465
NM_000426.3(LAMA2):c.8988+286A>G
NM_000426.3(LAMA2):c.9039T>C (p.Asp3013=) rs1057523899
NM_000426.3(LAMA2):c.9051A>G (p.Pro3017=) rs1057522162
NM_000426.3(LAMA2):c.910-14del rs769173629
NM_000426.3(LAMA2):c.9211+17C>T rs367830612
NM_000426.3(LAMA2):c.9212-11G>A rs770088527
NM_000426.3(LAMA2):c.922G>A (p.Glu308Lys) rs146462599
NM_000426.3(LAMA2):c.9339C>A (p.Gly3113=) rs182391310
NM_000426.3(LAMA2):c.9340G>A (p.Val3114Ile) rs200796753
NM_000426.3(LAMA2):c.99A>G (p.Ala33=) rs762858697

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