ClinVar Miner

List of variants in gene LAMA2 reported by Athena Diagnostics

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Gene type:
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Total variants: 95
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HGVS dbSNP gnomAD frequency
NM_000426.4(LAMA2):c.381C>A (p.Thr127=) rs4404787 0.95273
NM_000426.4(LAMA2):c.7830G>C (p.Val2610=) rs2229849 0.63102
NM_000426.4(LAMA2):c.5466A>G (p.Glu1822=) rs3749877 0.50817
NM_000426.4(LAMA2):c.7760= (p.Ala2587=) rs2229848 0.37054
NM_000426.4(LAMA2):c.2799A>G (p.Gln933=) rs1027199 0.26612
NM_000426.4(LAMA2):c.1856G>A (p.Arg619His) rs3816665 0.25123
NM_000426.4(LAMA2):c.156C>T (p.Ile52=) rs1140366 0.08417
NM_000426.4(LAMA2):c.4956C>G (p.Thr1652=) rs17057184 0.08154
NM_000426.4(LAMA2):c.6274+4C>T rs73775410 0.02805
NM_000426.4(LAMA2):c.8028T>C (p.Asn2676=) rs35313209 0.02285
NM_000426.4(LAMA2):c.8528A>G (p.Asn2843Ser) rs73599293 0.02027
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.7431A>T (p.Arg2477Ser) rs34367843 0.00850
NM_000426.4(LAMA2):c.1403C>G (p.Ala468Gly) rs111695726 0.00720
NM_000426.4(LAMA2):c.4437-5T>A rs41285288 0.00557
NM_000426.4(LAMA2):c.4470C>T (p.Asp1490=) rs35089085 0.00547
NM_000426.4(LAMA2):c.1634T>A (p.Leu545Gln) rs118083923 0.00348
NM_000426.4(LAMA2):c.4487C>T (p.Ala1496Val) rs147077184 0.00338
NM_000426.4(LAMA2):c.5909G>C (p.Cys1970Ser) rs148451013 0.00314
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.675C>T (p.Ala225=) rs139665175 0.00298
NM_000426.4(LAMA2):c.5247C>T (p.Ala1749=) rs149951387 0.00271
NM_000426.4(LAMA2):c.411G>A (p.Ala137=) rs149347601 0.00224
NM_000426.4(LAMA2):c.8755C>T (p.Pro2919Ser) rs143026295 0.00224
NM_000426.4(LAMA2):c.6429+8C>A rs199773264 0.00220
NM_000426.4(LAMA2):c.2430A>C (p.Pro810=) rs147572139 0.00185
NM_000426.4(LAMA2):c.1621A>G (p.Ser541Gly) rs141363186 0.00175
NM_000426.4(LAMA2):c.1308T>G (p.Gly436=) rs41285286 0.00162
NM_000426.4(LAMA2):c.8692A>C (p.Arg2898=) rs200718262 0.00121
NM_000426.4(LAMA2):c.1650C>T (p.Gly550=) rs899353 0.00120
NM_000426.4(LAMA2):c.1814C>T (p.Thr605Ile) rs112388307 0.00096
NM_000426.4(LAMA2):c.922G>A (p.Glu308Lys) rs146462599 0.00092
NM_000426.4(LAMA2):c.8586T>C (p.Tyr2862=) rs142451929 0.00074
NM_000426.4(LAMA2):c.3532G>A (p.Ala1178Thr) rs34505698 0.00066
NM_000426.4(LAMA2):c.1400A>G (p.Lys467Arg) rs138162760 0.00065
NM_000426.4(LAMA2):c.4740C>A (p.Gly1580=) rs371629354 0.00034
NM_000426.4(LAMA2):c.2121C>T (p.Ser707=) rs145622088 0.00027
NM_000426.4(LAMA2):c.5689G>A (p.Ala1897Thr) rs200518204 0.00021
NM_000426.4(LAMA2):c.2325C>A (p.Asn775Lys) rs139351727 0.00019
NM_000426.4(LAMA2):c.4909G>A (p.Glu1637Lys) rs138303386 0.00019
NM_000426.4(LAMA2):c.7057C>T (p.Arg2353Cys) rs145885540 0.00016
NM_000426.4(LAMA2):c.1873A>G (p.Ile625Val) rs141658354 0.00015
NM_000426.4(LAMA2):c.3628A>G (p.Ile1210Val) rs147291222 0.00014
NM_000426.4(LAMA2):c.4969G>A (p.Val1657Met) rs370971334 0.00014
NM_000426.4(LAMA2):c.5291A>G (p.Glu1764Gly) rs141950826 0.00014
NM_000426.4(LAMA2):c.7395T>C (p.Asp2465=) rs140483001 0.00014
NM_000426.4(LAMA2):c.8011C>A (p.Pro2671Thr) rs780695627 0.00014
NM_000426.4(LAMA2):c.9188C>A (p.Pro3063His) rs151285465 0.00014
NM_000426.4(LAMA2):c.8147G>A (p.Arg2716His) rs142781107 0.00011
NM_000426.4(LAMA2):c.4436+8T>C rs192650285 0.00009
NM_000426.4(LAMA2):c.7118C>T (p.Ser2373Leu) rs758887080 0.00007
NM_000426.4(LAMA2):c.1550A>T (p.Glu517Val) rs372358704 0.00006
NM_000426.4(LAMA2):c.479A>T (p.Asp160Val) rs147398243 0.00006
NM_000426.4(LAMA2):c.1586G>A (p.Ser529Asn) rs370691060 0.00005
NM_000426.4(LAMA2):c.4983C>T (p.Gly1661=) rs772192888 0.00004
NM_000426.4(LAMA2):c.5050G>A (p.Glu1684Lys) rs201632009 0.00004
NM_000426.4(LAMA2):c.6539A>T (p.Asp2180Val) rs567385461 0.00004
NM_000426.4(LAMA2):c.9060G>A (p.Leu3020=) rs368896579 0.00004
NM_000426.4(LAMA2):c.2477G>A (p.Arg826Gln) rs759973830 0.00003
NM_000426.4(LAMA2):c.6518A>T (p.Asn2173Ile) rs529110314 0.00003
NM_000426.4(LAMA2):c.112+1G>A rs398123367 0.00001
NM_000426.4(LAMA2):c.1623T>A (p.Ser541Arg) rs1344650184 0.00001
NM_000426.4(LAMA2):c.1681T>G (p.Leu561Val) rs765515681 0.00001
NM_000426.4(LAMA2):c.2376C>T (p.Phe792=) rs150046431 0.00001
NM_000426.4(LAMA2):c.2794A>G (p.Ser932Gly) rs761539740 0.00001
NM_000426.4(LAMA2):c.488A>T (p.Tyr163Phe) rs201175472 0.00001
NM_000426.4(LAMA2):c.5234+1G>A rs781376927 0.00001
NM_000426.4(LAMA2):c.5899G>T (p.Ala1967Ser) rs762129616 0.00001
NM_000426.4(LAMA2):c.6079C>A (p.Pro2027Thr) rs374006928 0.00001
NM_000426.4(LAMA2):c.6332A>T (p.Asp2111Val) rs371697379 0.00001
NM_000426.4(LAMA2):c.6659C>T (p.Pro2220Leu) rs367665458 0.00001
NM_000426.4(LAMA2):c.7074C>A (p.Tyr2358Ter) rs762806915 0.00001
NM_000426.4(LAMA2):c.7346T>C (p.Ile2449Thr) rs1156828795 0.00001
NM_000426.4(LAMA2):c.122C>T (p.Pro41Leu)
NM_000426.4(LAMA2):c.1262C>A (p.Ser421Tyr) rs775603569
NM_000426.4(LAMA2):c.2239G>T (p.Gly747Cys) rs145940188
NM_000426.4(LAMA2):c.2383G>T (p.Glu795Ter) rs149896793
NM_000426.4(LAMA2):c.3296A>G (p.Asn1099Ser) rs35065563
NM_000426.4(LAMA2):c.3317G>A (p.Cys1106Tyr) rs371548755
NM_000426.4(LAMA2):c.3570T>C (p.Ala1190=) rs373757863
NM_000426.4(LAMA2):c.3770T>A (p.Ile1257Asn)
NM_000426.4(LAMA2):c.3924+2T>C rs1554269966
NM_000426.4(LAMA2):c.3933G>C (p.Trp1311Cys)
NM_000426.4(LAMA2):c.4321C>A (p.His1441Asn) rs1562477412
NM_000426.4(LAMA2):c.4909G>C (p.Glu1637Gln) rs138303386
NM_000426.4(LAMA2):c.5072-6del rs398123376
NM_000426.4(LAMA2):c.5122G>C (p.Glu1708Gln)
NM_000426.4(LAMA2):c.5284C>G (p.Arg1762Gly) rs746492572
NM_000426.4(LAMA2):c.6764T>C (p.Ile2255Thr) rs951339046
NM_000426.4(LAMA2):c.6952T>A (p.Phe2318Ile) rs757197871
NM_000426.4(LAMA2):c.8244+3_8244+6del rs746678525
NM_000426.4(LAMA2):c.8857G>A (p.Val2953Ile) rs1211031170
NM_000426.4(LAMA2):c.9101_9104dup (p.His3035fs) rs398123390

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