ClinVar Miner

List of variants in gene LAMA2 reported by Athena Diagnostics Inc

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Total variants: 65
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HGVS dbSNP
NM_000426.3(LAMA2):c.1262C>A (p.Ser421Tyr)
NM_000426.3(LAMA2):c.1308T>G (p.Gly436=) rs41285286
NM_000426.3(LAMA2):c.1400A>G (p.Lys467Arg) rs138162760
NM_000426.3(LAMA2):c.1403C>G (p.Ala468Gly) rs111695726
NM_000426.3(LAMA2):c.156C>T (p.Ile52=) rs1140366
NM_000426.3(LAMA2):c.1586G>A (p.Ser529Asn) rs370691060
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.1650C>T (p.Gly550=) rs899353
NM_000426.3(LAMA2):c.1681T>G (p.Leu561Val)
NM_000426.3(LAMA2):c.1856G>A (p.Arg619His) rs3816665
NM_000426.3(LAMA2):c.1873A>G (p.Ile625Val) rs141658354
NM_000426.3(LAMA2):c.2430A>C (p.Pro810=) rs147572139
NM_000426.3(LAMA2):c.2477G>A (p.Arg826Gln) rs759973830
NM_000426.3(LAMA2):c.2794A>G (p.Ser932Gly) rs761539740
NM_000426.3(LAMA2):c.2799A>G (p.Gln933=) rs1027199
NM_000426.3(LAMA2):c.3296A>G (p.Asn1099Ser) rs35065563
NM_000426.3(LAMA2):c.3317G>A (p.Cys1106Tyr)
NM_000426.3(LAMA2):c.3532G>A (p.Ala1178Thr) rs34505698
NM_000426.3(LAMA2):c.3570T>C (p.Ala1190=)
NM_000426.3(LAMA2):c.381C>A (p.Thr127=) rs4404787
NM_000426.3(LAMA2):c.3924+2T>C rs1554269966
NM_000426.3(LAMA2):c.411G>A (p.Ala137=) rs149347601
NM_000426.3(LAMA2):c.4321C>A (p.His1441Asn)
NM_000426.3(LAMA2):c.4437-5T>A rs41285288
NM_000426.3(LAMA2):c.4487C>T (p.Ala1496Val) rs147077184
NM_000426.3(LAMA2):c.488A>T (p.Tyr163Phe) rs201175472
NM_000426.3(LAMA2):c.4909G>A (p.Glu1637Lys) rs138303386
NM_000426.3(LAMA2):c.4956C>G (p.Thr1652=) rs17057184
NM_000426.3(LAMA2):c.4969G>A (p.Val1657Met) rs370971334
NM_000426.3(LAMA2):c.5234+1G>A rs781376927
NM_000426.3(LAMA2):c.5284C>G (p.Arg1762Gly) rs746492572
NM_000426.3(LAMA2):c.5291A>G (p.Glu1764Gly) rs141950826
NM_000426.3(LAMA2):c.5466A>G (p.Glu1822=) rs3749877
NM_000426.3(LAMA2):c.5689G>A (p.Ala1897Thr) rs200518204
NM_000426.3(LAMA2):c.5909G>C (p.Cys1970Ser) rs148451013
NM_000426.3(LAMA2):c.6079C>A (p.Pro2027Thr)
NM_000426.3(LAMA2):c.6150T>C (p.Asp2050=) rs114766691
NM_000426.3(LAMA2):c.6158C>T (p.Ala2053Val)
NM_000426.3(LAMA2):c.6161A>G (p.Gln2054Arg) rs56035053
NM_000426.3(LAMA2):c.6274+4C>T rs73775410
NM_000426.3(LAMA2):c.6429+8C>A rs199773264
NM_000426.3(LAMA2):c.6518A>T (p.Asn2173Ile)
NM_000426.3(LAMA2):c.6539A>T (p.Asp2180Val) rs567385461
NM_000426.3(LAMA2):c.6659C>T (p.Pro2220Leu) rs367665458
NM_000426.3(LAMA2):c.675C>T (p.Ala225=) rs139665175
NM_000426.3(LAMA2):c.6764T>C (p.Ile2255Thr)
NM_000426.3(LAMA2):c.6952T>A (p.Phe2318Ile) rs757197871
NM_000426.3(LAMA2):c.7057C>T (p.Arg2353Cys) rs145885540
NM_000426.3(LAMA2):c.7074C>A (p.Tyr2358Ter) rs762806915
NM_000426.3(LAMA2):c.7346T>C (p.Ile2449Thr) rs1156828795
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.7760T>C (p.Val2587Ala) rs2229848
NM_000426.3(LAMA2):c.7830G>C (p.Val2610=) rs2229849
NM_000426.3(LAMA2):c.8011C>A (p.Pro2671Thr) rs780695627
NM_000426.3(LAMA2):c.8028T>C (p.Asn2676=) rs35313209
NM_000426.3(LAMA2):c.8147G>A (p.Arg2716His) rs142781107
NM_000426.3(LAMA2):c.8244+3_8244+6delAAGT rs746678525
NM_000426.3(LAMA2):c.8528A>G (p.Asn2843Ser) rs73599293
NM_000426.3(LAMA2):c.8548-10T>C rs113644365
NM_000426.3(LAMA2):c.8586T>C (p.Tyr2862=) rs142451929
NM_000426.3(LAMA2):c.8692A>C (p.Arg2898=) rs200718262
NM_000426.3(LAMA2):c.9101_9104dupAACA (p.His3035Glnfs) rs398123390
NM_000426.3(LAMA2):c.922G>A (p.Glu308Lys) rs146462599

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