ClinVar Miner

List of variants in gene LAMA2 reported by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Total variants: 173
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HGVS dbSNP
NM_000426.3(LAMA2):c.101A>G (p.His34Arg) rs398123366
NM_000426.3(LAMA2):c.1032_1042del (p.Cys344fs) rs886044344
NM_000426.3(LAMA2):c.112+1G>A rs398123367
NM_000426.3(LAMA2):c.13G>A (p.Ala5Thr) rs367622987
NM_000426.3(LAMA2):c.1546G>A (p.Asp516Asn) rs141000358
NM_000426.3(LAMA2):c.156C>T (p.Ile52=) rs1140366
NM_000426.3(LAMA2):c.1580G>A (p.Cys527Tyr) rs121913574
NM_000426.3(LAMA2):c.1610_1611del (p.Ile537fs) rs886043374
NM_000426.3(LAMA2):c.1621A>G (p.Ser541Gly) rs141363186
NM_000426.3(LAMA2):c.1634T>A (p.Leu545Gln) rs118083923
NM_000426.3(LAMA2):c.1645C>T (p.Pro549Ser) rs139070796
NM_000426.3(LAMA2):c.1701C>T (p.Ile567=) rs111381107
NM_000426.3(LAMA2):c.1782+10C>T rs200030296
NM_000426.3(LAMA2):c.1798G>A (p.Gly600Arg) rs36044314
NM_000426.3(LAMA2):c.1816A>G (p.Ile606Val) rs113022759
NM_000426.3(LAMA2):c.184G>T (p.Gly62Ter) rs398123368
NM_000426.3(LAMA2):c.1854_1861dup (p.Leu621fs) rs202247791
NM_000426.3(LAMA2):c.1855_1856insATGTTCAC (p.Arg619fs) rs797044643
NM_000426.3(LAMA2):c.1856G>A (p.Arg619His) rs3816665
NM_000426.3(LAMA2):c.1882G>A (p.Glu628Lys) rs794727088
NM_000426.3(LAMA2):c.2037G>C (p.Ala679=) rs398123369
NM_000426.3(LAMA2):c.2049_2050delAG rs202247790
NM_000426.3(LAMA2):c.2115T>G (p.Leu705=) rs149753273
NM_000426.3(LAMA2):c.2186G>T (p.Gly729Val) rs763338640
NM_000426.3(LAMA2):c.2209-6_2209-3delTCTC rs769187963
NM_000426.3(LAMA2):c.2288C>T (p.Ala763Val) rs141521127
NM_000426.3(LAMA2):c.2289G>A (p.Ala763=) rs754496465
NM_000426.3(LAMA2):c.2304C>T (p.Asp768=) rs142126511
NM_000426.3(LAMA2):c.2318G>A (p.Cys773Tyr) rs746327071
NM_000426.3(LAMA2):c.2324A>G (p.Asn775Ser) rs1562399416
NM_000426.3(LAMA2):c.2352T>G (p.Tyr784Ter) rs886044330
NM_000426.3(LAMA2):c.2375T>C (p.Phe792Ser) rs398123370
NM_000426.3(LAMA2):c.2382C>T (p.Gly794=) rs147744763
NM_000426.3(LAMA2):c.2462C>T (p.Thr821Met) rs117422805
NM_000426.3(LAMA2):c.2476C>T (p.Arg826Trp) rs118147866
NM_000426.3(LAMA2):c.255C>T (p.Ile85=) rs142083777
NM_000426.3(LAMA2):c.2584T>C (p.Cys862Arg) rs121913573
NM_000426.3(LAMA2):c.2736G>A (p.Ala912=) rs142671449
NM_000426.3(LAMA2):c.2749+1G>C rs759555791
NM_000426.3(LAMA2):c.2750-1G>C rs9492297
NM_000426.3(LAMA2):c.2756G>T (p.Arg919Leu) rs35277491
NM_000426.3(LAMA2):c.2799A>G (p.Gln933=) rs1027199
NM_000426.3(LAMA2):c.2831A>G (p.Gln944Arg) rs141920360
NM_000426.3(LAMA2):c.284-4A>G rs185151902
NM_000426.3(LAMA2):c.2916T>G (p.Phe972Leu) rs763840955
NM_000426.3(LAMA2):c.2962C>T (p.Gln988Ter) rs398123371
NM_000426.3(LAMA2):c.2993G>A (p.Arg998His) rs144946631
NM_000426.3(LAMA2):c.3014A>G (p.Asn1005Ser) rs139244736
NM_000426.3(LAMA2):c.3175-32_3175-31delGT rs372962551
NM_000426.3(LAMA2):c.3237C>A (p.Cys1079Ter) rs1554268940
NM_000426.3(LAMA2):c.3411+13G>A rs3798663
NM_000426.3(LAMA2):c.3412G>A (p.Val1138Met) rs2306942
NM_000426.3(LAMA2):c.3532G>A (p.Ala1178Thr) rs34505698
NM_000426.3(LAMA2):c.3556-15T>G rs17741922
NM_000426.3(LAMA2):c.3585A>G (p.Leu1195=) rs780444488
NM_000426.3(LAMA2):c.3623_3645del (p.Lys1208fs) rs727503992
NM_000426.3(LAMA2):c.3630del (p.Ile1210fs) rs398123372
NM_000426.3(LAMA2):c.3645A>G (p.Pro1215=) rs794727396
NM_000426.3(LAMA2):c.3685C>T (p.His1229Tyr) rs143247439
NM_000426.3(LAMA2):c.3718C>T (p.Gln1240Ter) rs121913569
NM_000426.3(LAMA2):c.381C>A (p.Thr127=) rs4404787
NM_000426.3(LAMA2):c.3924+2T>C rs1554269966
NM_000426.3(LAMA2):c.396+1G>T rs770617208
NM_000426.3(LAMA2):c.3976C>T (p.Arg1326Ter) rs398123373
NM_000426.3(LAMA2):c.3979_3985dup (p.Phe1329Ter) rs886042847
NM_000426.3(LAMA2):c.4048C>T (p.Arg1350Ter) rs756854513
NM_000426.3(LAMA2):c.411G>A (p.Ala137=) rs149347601
NM_000426.3(LAMA2):c.4148C>T (p.Pro1383Leu) rs1233536347
NM_000426.3(LAMA2):c.4166T>C (p.Leu1389Pro) rs752934825
NM_000426.3(LAMA2):c.4312-19_4312-17delTCT rs398123374
NM_000426.3(LAMA2):c.4437-5T>A rs41285288
NM_000426.3(LAMA2):c.444dup (p.Pro149fs) rs759516529
NM_000426.3(LAMA2):c.4470C>T (p.Asp1490=) rs35089085
NM_000426.3(LAMA2):c.4487C>T (p.Ala1496Val) rs147077184
NM_000426.3(LAMA2):c.4523+19C>T rs17057158
NM_000426.3(LAMA2):c.4523+1G>A rs398123375
NM_000426.3(LAMA2):c.4620C>A (p.Asp1540Glu)
NM_000426.3(LAMA2):c.4750G>A (p.Gly1584Ser) rs117781224
NM_000426.3(LAMA2):c.479A>T (p.Asp160Val) rs147398243
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.4956C>G (p.Thr1652=) rs17057184
NM_000426.3(LAMA2):c.4959+6G>T rs148060790
NM_000426.3(LAMA2):c.4969G>A (p.Val1657Met) rs370971334
NM_000426.3(LAMA2):c.5050G>T (p.Glu1684Ter) rs201632009
NM_000426.3(LAMA2):c.5072-6delC rs398123376
NM_000426.3(LAMA2):c.5116C>T (p.Arg1706Ter) rs758775001
NM_000426.3(LAMA2):c.5247C>T (p.Ala1749=) rs149951387
NM_000426.3(LAMA2):c.524_534dup (p.Leu179delinsSerAlaTer) rs797044728
NM_000426.3(LAMA2):c.5260del (p.Lys1753_Val1754insTer) rs794727594
NM_000426.3(LAMA2):c.5466A>G (p.Glu1822=) rs3749877
NM_000426.3(LAMA2):c.5469C>T (p.Ser1823=) rs753886576
NM_000426.3(LAMA2):c.5502G>A (p.Glu1834=) rs3749878
NM_000426.3(LAMA2):c.5518G>A (p.Asp1840Asn) rs759350875
NM_000426.3(LAMA2):c.5530C>A (p.Arg1844Ser) rs56173620
NM_000426.3(LAMA2):c.5562+5G>C rs771046502
NM_000426.3(LAMA2):c.5601T>G (p.Ser1867=) rs780368037
NM_000426.3(LAMA2):c.5605G>T (p.Glu1869Ter) rs746762473
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.5706_5712del (p.Asp1902fs) rs398123377
NM_000426.3(LAMA2):c.5914C>T (p.Gln1972Ter) rs398123378
NM_000426.3(LAMA2):c.595T>A (p.Cys199Ser) rs886043693
NM_000426.3(LAMA2):c.5969-4G>A rs566302197
NM_000426.3(LAMA2):c.6002G>A (p.Arg2001Lys) rs151009169
NM_000426.3(LAMA2):c.6011del (p.Asn2004fs) rs398123379
NM_000426.3(LAMA2):c.6038del (p.Leu2012_Leu2013insTer) rs398123380
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.6237G>A (p.Thr2079=) rs2297738
NM_000426.3(LAMA2):c.623C>A (p.Pro208His) rs183890063
NM_000426.3(LAMA2):c.6268+5G>C rs182064878
NM_000426.3(LAMA2):c.6322C>T (p.Arg2108Trp) rs139824017
NM_000426.3(LAMA2):c.6345C>T (p.Pro2115=) rs200364660
NM_000426.3(LAMA2):c.6426T>C (p.Asn2142=) rs150730793
NM_000426.3(LAMA2):c.6429+8C>A rs199773264
NM_000426.3(LAMA2):c.6444G>A (p.Val2148=) rs781231694
NM_000426.3(LAMA2):c.6551T>C (p.Phe2184Ser) rs398123381
NM_000426.3(LAMA2):c.6563G>A (p.Ser2188Asn) rs372592018
NM_000426.3(LAMA2):c.6629T>C (p.Val2210Ala) rs78880369
NM_000426.3(LAMA2):c.6649G>A (p.Val2217Ile) rs147857398
NM_000426.3(LAMA2):c.6697G>A (p.Val2233Ile) rs150945378
NM_000426.3(LAMA2):c.675C>T (p.Ala225=) rs139665175
NM_000426.3(LAMA2):c.6786G>A (p.Ser2262=) rs398123382
NM_000426.3(LAMA2):c.6816T>C (p.Asp2272=) rs794727687
NM_000426.3(LAMA2):c.6832A>G (p.Met2278Val) rs146854942
NM_000426.3(LAMA2):c.6955C>T (p.Arg2319Ter) rs398123383
NM_000426.3(LAMA2):c.7111T>G (p.Phe2371Val) rs150644209
NM_000426.3(LAMA2):c.713C>A (p.Ala238Asp) rs398123384
NM_000426.3(LAMA2):c.7147C>T (p.Arg2383Ter) rs121913576
NM_000426.3(LAMA2):c.7155+1G>A rs886043692
NM_000426.3(LAMA2):c.7250A>G (p.His2417Arg) rs147185142
NM_000426.3(LAMA2):c.7277_7278CT[1] (p.Leu2427fs) rs398123385
NM_000426.3(LAMA2):c.7288A>C (p.Ile2430Leu) rs1562589458
NM_000426.3(LAMA2):c.7300+10T>A rs200469923
NM_000426.3(LAMA2):c.7395T>C (p.Asp2465=) rs140483001
NM_000426.3(LAMA2):c.7431A>T (p.Arg2477Ser) rs34367843
NM_000426.3(LAMA2):c.7439+1G>A rs886043630
NM_000426.3(LAMA2):c.7440-20delT rs398123386
NM_000426.3(LAMA2):c.7440-9G>A rs369558532
NM_000426.3(LAMA2):c.7536del (p.Asp2513fs) rs398123387
NM_000426.3(LAMA2):c.7732C>T (p.Arg2578Ter) rs121913572
NM_000426.3(LAMA2):c.7760= (p.Val2587=) rs2229848
NM_000426.3(LAMA2):c.7810C>T (p.Arg2604Ter) rs766920075
NM_000426.3(LAMA2):c.7830G>C (p.Val2610=) rs2229849
NM_000426.3(LAMA2):c.7845G>A (p.Pro2615=) rs2229850
NM_000426.3(LAMA2):c.7906A>G (p.Thr2636Ala) rs2244008
NM_000426.3(LAMA2):c.7965C>A (p.Ile2655=) rs141101234
NM_000426.3(LAMA2):c.7991del (p.Gly2664fs) rs886039541
NM_000426.3(LAMA2):c.8124T>A (p.Gly2708=) rs34997144
NM_000426.3(LAMA2):c.8155G>T (p.Glu2719Ter) rs1289855948
NM_000426.3(LAMA2):c.817A>T (p.Arg273Ter) rs886043648
NM_000426.3(LAMA2):c.8211A>C (p.Pro2737=) rs369596190
NM_000426.3(LAMA2):c.8282T>C (p.Ile2761Thr) rs115650537
NM_000426.3(LAMA2):c.830C>T (p.Ser277Leu) rs398123388
NM_000426.3(LAMA2):c.8467C>T (p.Pro2823Ser) rs151334775
NM_000426.3(LAMA2):c.8497G>T (p.Asp2833Tyr) rs794727815
NM_000426.3(LAMA2):c.8548-10T>C rs113644365
NM_000426.3(LAMA2):c.8556_8558del (p.Ile2852del) rs398123389
NM_000426.3(LAMA2):c.8669dup (p.Leu2890fs) rs1554316216
NM_000426.3(LAMA2):c.8692A>C (p.Arg2898=) rs200718262
NM_000426.3(LAMA2):c.8728G>A (p.Val2910Ile) rs141479751
NM_000426.3(LAMA2):c.8755C>T (p.Pro2919Ser) rs143026295
NM_000426.3(LAMA2):c.8842G>A (p.Gly2948Ser) rs143638361
NM_000426.3(LAMA2):c.8918C>T (p.Thr2973Met) rs145842163
NM_000426.3(LAMA2):c.8920A>T (p.Thr2974Ser) rs140202046
NM_000426.3(LAMA2):c.8982T>C (p.Asp2994=) rs79374915
NM_000426.3(LAMA2):c.9101_9104dup (p.His3035fs) rs398123390
NM_000426.3(LAMA2):c.9211+6T>C rs201375881
NM_000426.3(LAMA2):c.9212-1G>A rs398123391
NM_000426.3(LAMA2):c.9340G>A (p.Val3114Ile) rs200796753
NM_001079823.2(LAMA2):c.5749A>T (p.Ile1917Phe) rs727503993
NM_001079823.2(LAMA2):c.8114G>A (p.Arg2705His) rs199714288

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