ClinVar Miner

List of variants in gene LAMA2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 100
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HGVS dbSNP gnomAD frequency
NM_000426.4(LAMA2):c.1467+38C>T rs78299321 0.02120
NM_000426.4(LAMA2):c.1491T>C (p.Cys497=) rs2306220 0.01733
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.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.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.1621A>G (p.Ser541Gly) rs141363186 0.00175
NM_000426.4(LAMA2):c.6279C>T (p.Ala2093=) rs141190803 0.00173
NM_000426.4(LAMA2):c.1308T>G (p.Gly436=) rs41285286 0.00165
NM_000426.4(LAMA2):c.7640G>A (p.Gly2547Glu) rs115488979 0.00165
NM_000426.4(LAMA2):c.7111T>G (p.Phe2371Val) rs150644209 0.00164
NM_000426.4(LAMA2):c.8728G>A (p.Val2910Ile) rs141479751 0.00150
NM_000426.4(LAMA2):c.1782+14T>C rs191215452 0.00147
NM_000426.4(LAMA2):c.74C>T (p.Pro25Leu) rs145310035 0.00147
NM_000426.4(LAMA2):c.4960-16G>A rs9483026 0.00133
NM_000426.4(LAMA2):c.1814C>T (p.Thr605Ile) rs112388307 0.00103
NM_000426.4(LAMA2):c.4349G>A (p.Arg1450Gln) rs148905630 0.00099
NM_000426.4(LAMA2):c.6649G>A (p.Val2217Ile) rs147857398 0.00093
NM_000426.4(LAMA2):c.1782+10C>T rs200030296 0.00091
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.5021G>A (p.Arg1674Lys) rs143333246 0.00090
NM_000426.4(LAMA2):c.6708-3A>C rs112637707 0.00087
NM_000426.4(LAMA2):c.7869A>G (p.Glu2623=) rs140658201 0.00074
NM_000426.4(LAMA2):c.8586T>C (p.Tyr2862=) rs142451929 0.00074
NM_000426.4(LAMA2):c.5121C>T (p.Asp1707=) rs151199929 0.00064
NM_000426.4(LAMA2):c.3154A>G (p.Ser1052Gly) rs149165006 0.00061
NM_000426.4(LAMA2):c.6629T>C (p.Val2210Ala) rs78880369 0.00060
NM_000426.4(LAMA2):c.7300+10T>A rs200469923 0.00056
NM_000426.4(LAMA2):c.3014A>G (p.Asn1005Ser) rs139244736 0.00052
NM_000426.4(LAMA2):c.8761G>A (p.Asp2921Asn) rs139159258 0.00050
NM_000426.4(LAMA2):c.4176+9C>T rs117116822 0.00042
NM_000426.4(LAMA2):c.4944C>T (p.Asn1648=) rs111632017 0.00037
NM_000426.4(LAMA2):c.4926A>G (p.Thr1642=) rs62421010 0.00034
NM_000426.4(LAMA2):c.6708-13C>T rs375474916 0.00033
NM_000426.4(LAMA2):c.2121C>T (p.Ser707=) rs145622088 0.00029
NM_000426.4(LAMA2):c.5509G>A (p.Asp1837Asn) rs749423866 0.00026
NM_000426.4(LAMA2):c.7983C>T (p.Phe2661=) rs150184189 0.00025
NM_000426.4(LAMA2):c.6002G>A (p.Arg2001Lys) rs151009169 0.00023
NM_000426.4(LAMA2):c.3213A>G (p.Gln1071=) rs372938168 0.00021
NM_000426.4(LAMA2):c.5558T>G (p.Ile1853Arg) rs141911213 0.00020
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.7659A>G (p.Ser2553=) rs149867744 0.00015
NM_000426.4(LAMA2):c.7395T>C (p.Asp2465=) rs140483001 0.00014
NM_000426.4(LAMA2):c.879C>T (p.Ala293=) rs148419866 0.00012
NM_000426.4(LAMA2):c.3004G>A (p.Gly1002Ser) rs200953311 0.00011
NM_000426.4(LAMA2):c.3597T>C (p.Asp1199=) rs199904029 0.00011
NM_000426.4(LAMA2):c.4992C>T (p.Thr1664=) rs143078882 0.00011
NM_000426.4(LAMA2):c.5769A>G (p.Ala1923=) rs200582139 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.7452-9A>G rs748647936 0.00008
NM_000426.4(LAMA2):c.7772A>G (p.Asn2591Ser) rs200095274 0.00007
NM_000426.4(LAMA2):c.8610C>T (p.Thr2870=) rs199709403 0.00006
NM_000426.4(LAMA2):c.5969-4G>A rs566302197 0.00005
NM_000426.4(LAMA2):c.6870G>A (p.Lys2290=) rs748561685 0.00005
NM_000426.4(LAMA2):c.9367_*1dup (p.Ter3123=) rs772463361 0.00005
NM_000426.4(LAMA2):c.5280G>A (p.Glu1760=) rs376693904 0.00004
NM_000426.4(LAMA2):c.6539A>T (p.Asp2180Val) rs567385461 0.00004
NM_000426.4(LAMA2):c.1207-10T>A rs779863501 0.00003
NM_000426.4(LAMA2):c.6429+10T>G rs770063449 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.8385C>T (p.Thr2795=) rs142445491 0.00003
NM_000426.4(LAMA2):c.3279C>T (p.Cys1093=) rs371376404 0.00002
NM_000426.4(LAMA2):c.4164C>T (p.Gly1388=) rs766082530 0.00002
NM_000426.4(LAMA2):c.5072-10C>A rs552989582 0.00002
NM_000426.4(LAMA2):c.2001T>C (p.Phe667=) rs138600346 0.00001
NM_000426.4(LAMA2):c.2376C>T (p.Phe792=) rs150046431 0.00001
NM_000426.4(LAMA2):c.2749+24C>A rs886038292 0.00001
NM_000426.4(LAMA2):c.3175-22G>A rs777129293 0.00001
NM_000426.4(LAMA2):c.4734C>T (p.Cys1578=) rs1401689375 0.00001
NM_000426.4(LAMA2):c.6531T>A (p.Ala2177=) rs1244983337 0.00001
NM_000426.4(LAMA2):c.6927C>T (p.Asp2309=) rs575850136 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.2756G>T (p.Arg919Leu) rs35277491
NM_000426.4(LAMA2):c.2857-14T>A rs535718824
NM_000426.4(LAMA2):c.2857-47G>A
NM_000426.4(LAMA2):c.2857-48C>T
NM_000426.4(LAMA2):c.3168T>C (p.Gly1056=)
NM_000426.4(LAMA2):c.3429C>T (p.Ile1143=) rs200646230
NM_000426.4(LAMA2):c.3969T>C (p.Thr1323=) rs112327654
NM_000426.4(LAMA2):c.5140T>C (p.Leu1714=) rs572008421
NM_000426.4(LAMA2):c.5235-28T>C
NM_000426.4(LAMA2):c.5530C>T (p.Arg1844Cys) rs56173620
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.8076-24A>G rs886038296
NM_000426.4(LAMA2):c.9211+21C>A rs886038297
NM_000426.4(LAMA2):c.9318C>G (p.Ala3106=) rs1342516974

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