ClinVar Miner

List of variants in gene LAMA2 reported as benign by Genetic Services Laboratory, University of Chicago

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Gene type:
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Total variants: 15
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HGVS dbSNP
NM_000426.3(LAMA2):c.156C>T (p.Ile52=) rs1140366
NM_000426.3(LAMA2):c.1856G>A (p.Arg619His) rs3816665
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.3412G>A (p.Val1138Met) rs2306942
NM_000426.3(LAMA2):c.381C>A (p.Thr127=) rs4404787
NM_000426.3(LAMA2):c.4956C>G (p.Thr1652=) rs17057184
NM_000426.3(LAMA2):c.5466A>G (p.Glu1822=) rs3749877
NM_000426.3(LAMA2):c.5502G>A (p.Glu1834=) rs3749878
NM_000426.3(LAMA2):c.5688C>T (p.His1896=) rs573779258
NM_000426.3(LAMA2):c.6237G>A (p.Thr2079=) rs2297738
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.8755C>T (p.Pro2919Ser) rs143026295

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