ClinVar Miner

List of variants in gene LAMA2 reported as uncertain significance for not provided

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Gene type:
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Total variants: 146
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HGVS dbSNP
NM_000426.3(LAMA2):c.101A>G (p.His34Arg) rs398123366
NM_000426.3(LAMA2):c.1262C>A (p.Ser421Tyr)
NM_000426.3(LAMA2):c.1308T>G (p.Gly436=) rs41285286
NM_000426.3(LAMA2):c.1373G>A (p.Arg458Lys) rs140604077
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.1558T>A (p.Cys520Ser) rs886061046
NM_000426.3(LAMA2):c.1580G>A (p.Cys527Tyr) rs121913574
NM_000426.3(LAMA2):c.1621A>G (p.Ser541Gly) rs141363186
NM_000426.3(LAMA2):c.1645C>T (p.Pro549Ser) rs139070796
NM_000426.3(LAMA2):c.1670A>C (p.Gln557Pro) rs1333451961
NM_000426.3(LAMA2):c.1681T>G (p.Leu561Val)
NM_000426.3(LAMA2):c.1782+10C>T rs200030296
NM_000426.3(LAMA2):c.1792G>A (p.Val598Ile) rs753232836
NM_000426.3(LAMA2):c.1816A>G (p.Ile606Val) rs113022759
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.2054T>C (p.Leu685Pro) rs746641607
NM_000426.3(LAMA2):c.2084A>T (p.Asp695Val) rs762272518
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.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.2477G>A (p.Arg826Gln) rs759973830
NM_000426.3(LAMA2):c.255C>T (p.Ile85=) rs142083777
NM_000426.3(LAMA2):c.2564C>G (p.Pro855Arg) rs754714449
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.2767G>A (p.Gly923Ser) rs144492513
NM_000426.3(LAMA2):c.2780C>T (p.Ser927Phe) rs1085307732
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.2932G>A (p.Asp978Asn) rs202050052
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.3154A>G (p.Ser1052Gly) rs149165006
NM_000426.3(LAMA2):c.3317G>A (p.Cys1106Tyr)
NM_000426.3(LAMA2):c.3461G>T (p.Gly1154Val) rs922954882
NM_000426.3(LAMA2):c.3532G>A (p.Ala1178Thr) rs34505698
NM_000426.3(LAMA2):c.3585A>G (p.Leu1195=) rs780444488
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.3850G>C (p.Ala1284Pro) rs1085307846
NM_000426.3(LAMA2):c.4060A>G (p.Ile1354Val) rs143674727
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_4312-17del rs398123374
NM_000426.3(LAMA2):c.4321C>A (p.His1441Asn) rs1562477412
NM_000426.3(LAMA2):c.437C>T (p.Ser146Phe) rs143680577
NM_000426.3(LAMA2):c.4471G>A (p.Asp1491Asn) rs375640462
NM_000426.3(LAMA2):c.4487C>T (p.Ala1496Val) rs147077184
NM_000426.3(LAMA2):c.4620C>A (p.Asp1540Glu)
NM_000426.3(LAMA2):c.4646G>A (p.Arg1549Gln) rs778508100
NM_000426.3(LAMA2):c.4657A>G (p.Thr1553Ala) rs1450772080
NM_000426.3(LAMA2):c.479A>G (p.Asp160Gly) rs147398243
NM_000426.3(LAMA2):c.479A>T (p.Asp160Val) rs147398243
NM_000426.3(LAMA2):c.4909G>A (p.Glu1637Lys) rs138303386
NM_000426.3(LAMA2):c.4926A>G (p.Thr1642=) rs62421010
NM_000426.3(LAMA2):c.4959+6G>T rs148060790
NM_000426.3(LAMA2):c.4960-17C>A rs758048596
NM_000426.3(LAMA2):c.4969G>A (p.Val1657Met) rs370971334
NM_000426.3(LAMA2):c.518A>T (p.Asp173Val) rs767671585
NM_000426.3(LAMA2):c.525G>C (p.Glu175Asp) rs1554217596
NM_000426.3(LAMA2):c.5291A>G (p.Glu1764Gly) rs141950826
NM_000426.3(LAMA2):c.5469C>T (p.Ser1823=) rs753886576
NM_000426.3(LAMA2):c.5518G>A (p.Asp1840Asn) rs759350875
NM_000426.3(LAMA2):c.5530C>T (p.Arg1844Cys) rs56173620
NM_000426.3(LAMA2):c.5601T>G (p.Ser1867=) rs780368037
NM_000426.3(LAMA2):c.5833G>A (p.Ala1945Thr) rs3828736
NM_000426.3(LAMA2):c.595T>A (p.Cys199Ser) rs886043693
NM_000426.3(LAMA2):c.5978A>G (p.Asp1993Gly) rs752249871
NM_000426.3(LAMA2):c.6002G>A (p.Arg2001Lys) rs151009169
NM_000426.3(LAMA2):c.6047T>C (p.Leu2016Ser) rs773309064
NM_000426.3(LAMA2):c.6079C>A (p.Pro2027Thr)
NM_000426.3(LAMA2):c.6128A>G (p.Gln2043Arg) rs144155507
NM_000426.3(LAMA2):c.6158C>T (p.Ala2053Val) rs1562566133
NM_000426.3(LAMA2):c.6161A>G (p.Gln2054Arg) rs56035053
NM_000426.3(LAMA2):c.6195_6197GAA[2] (p.Lys2067del) rs758495000
NM_000426.3(LAMA2):c.623C>A (p.Pro208His) rs183890063
NM_000426.3(LAMA2):c.6268+5G>C rs182064878
NM_000426.3(LAMA2):c.6274+5G>T rs367765202
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.6421G>A (p.Ala2141Thr) rs768685078
NM_000426.3(LAMA2):c.6426T>C (p.Asn2142=) rs150730793
NM_000426.3(LAMA2):c.6444G>A (p.Val2148=) rs781231694
NM_000426.3(LAMA2):c.6518A>T (p.Asn2173Ile)
NM_000426.3(LAMA2):c.6539A>T (p.Asp2180Val) rs567385461
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.665G>C (p.Arg222Thr) rs1267371641
NM_000426.3(LAMA2):c.6697G>A (p.Val2233Ile) rs150945378
NM_000426.3(LAMA2):c.6708-3A>C rs112637707
NM_000426.3(LAMA2):c.670A>G (p.Ser224Gly) rs1085307718
NM_000426.3(LAMA2):c.6764T>C (p.Ile2255Thr)
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.7057C>T (p.Arg2353Cys) rs145885540
NM_000426.3(LAMA2):c.7111T>G (p.Phe2371Val) rs150644209
NM_000426.3(LAMA2):c.7112T>G (p.Phe2371Cys) rs201274841
NM_000426.3(LAMA2):c.713C>A (p.Ala238Asp) rs398123384
NM_000426.3(LAMA2):c.7250A>G (p.His2417Arg) rs147185142
NM_000426.3(LAMA2):c.7288A>C (p.Ile2430Leu) rs1562589458
NM_000426.3(LAMA2):c.7300+10T>A rs200469923
NM_000426.3(LAMA2):c.7390G>T (p.Ala2464Ser) rs1131691621
NM_000426.3(LAMA2):c.7395T>C (p.Asp2465=) rs140483001
NM_000426.3(LAMA2):c.7440-20del rs398123386
NM_000426.3(LAMA2):c.7440-9G>A rs369558532
NM_000426.3(LAMA2):c.7965C>A (p.Ile2655=) rs141101234
NM_000426.3(LAMA2):c.8076-7C>G rs555377928
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.848T>C (p.Val283Ala) rs376917587
NM_000426.3(LAMA2):c.8497G>T (p.Asp2833Tyr) rs794727815
NM_000426.3(LAMA2):c.8556_8558del (p.Ile2852del) rs398123389
NM_000426.3(LAMA2):c.855G>T (p.Gly285=) rs1008267864
NM_000426.3(LAMA2):c.8690G>A (p.Arg2897Gln) rs201696115
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.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.8988+15T>C rs201041465
NM_000426.3(LAMA2):c.9001G>C (p.Val3001Leu) rs189360899
NM_000426.3(LAMA2):c.9145C>G (p.Gln3049Glu) rs146525742
NM_000426.3(LAMA2):c.917G>A (p.Arg306His) rs1023922833
NM_000426.3(LAMA2):c.9211+6T>C rs201375881
NM_000426.3(LAMA2):c.922G>A (p.Glu308Lys) rs146462599
NM_000426.3(LAMA2):c.9253C>T rs121913571
NM_000426.3(LAMA2):c.9269_9283dup (p.Lys3095_Gly3096insThrLeuLysLeuThr) rs1554321191
NM_000426.3(LAMA2):c.9340G>A (p.Val3114Ile) rs200796753
NM_000426.3(LAMA2):c.946G>A (p.Asp316Asn) rs141340479
NM_001079823.2(LAMA2):c.5749A>T (p.Ile1917Phe) rs727503993
NM_001079823.2(LAMA2):c.8114G>A (p.Arg2705His) rs199714288

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