ClinVar Miner

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

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Total variants: 22
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HGVS dbSNP
NM_000426.3(LAMA2):c.1621A>G (p.Ser541Gly) rs141363186
NM_000426.3(LAMA2):c.1702A>G (p.Ser568Gly) rs754994339
NM_000426.3(LAMA2):c.2122G>A (p.Ala708Thr) rs777765933
NM_000426.3(LAMA2):c.2462C>T (p.Thr821Met) rs117422805
NM_000426.3(LAMA2):c.3110T>C (p.Ile1037Thr) rs797045679
NM_000426.3(LAMA2):c.3279C>T (p.Cys1093=) rs371376404
NM_000426.3(LAMA2):c.4487C>T (p.Ala1496Val) rs147077184
NM_000426.3(LAMA2):c.5021G>A (p.Arg1674Lys) rs143333246
NM_000426.3(LAMA2):c.5633C>T (p.Ser1878Phe) rs139586720
NM_000426.3(LAMA2):c.5670G>T (p.Val1890=) rs374587087
NM_000426.3(LAMA2):c.5675A>T (p.Gln1892Leu) rs779542581
NM_000426.3(LAMA2):c.6161A>G (p.Gln2054Arg) rs56035053
NM_000426.3(LAMA2):c.6268+5G>C rs182064878
NM_000426.3(LAMA2):c.6274+5G>A rs367765202
NM_000426.3(LAMA2):c.6539A>T (p.Asp2180Val) rs567385461
NM_000426.3(LAMA2):c.7088C>T (p.Thr2363Ile) rs371403343
NM_000426.3(LAMA2):c.7300+10T>A rs200469923
NM_000426.3(LAMA2):c.7369A>C (p.Asn2457His) rs797045680
NM_000426.3(LAMA2):c.7415G>T (p.Gly2472Val) rs200921233
NM_000426.3(LAMA2):c.8223G>A (p.Thr2741=) rs150596964
NM_000426.3(LAMA2):c.8524A>G (p.Ile2842Val) rs140178576
NM_000426.3(LAMA2):c.9254G>A (p.Arg3085Gln) rs776606476

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