ClinVar Miner

List of variants in gene LAMA2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_000426.4(LAMA2):c.7431A>T (p.Arg2477Ser) rs34367843 0.00914
NM_000426.4(LAMA2):c.2476C>T (p.Arg826Trp) rs118147866 0.00549
NM_000426.4(LAMA2):c.1634T>A (p.Leu545Gln) rs118083923 0.00359
NM_000426.4(LAMA2):c.4487C>T (p.Ala1496Val) rs147077184 0.00338
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.5633C>T (p.Ser1878Phe) rs139586720 0.00279
NM_000426.4(LAMA2):c.5247C>T (p.Ala1749=) rs149951387 0.00271
NM_000426.4(LAMA2):c.6429+8C>A rs199773264 0.00238
NM_000426.4(LAMA2):c.4959+6G>T rs148060790 0.00236
NM_000426.4(LAMA2):c.411G>A (p.Ala137=) rs149347601 0.00206
NM_000426.4(LAMA2):c.1621A>G (p.Ser541Gly) rs141363186 0.00175
NM_000426.4(LAMA2):c.2462C>T (p.Thr821Met) rs117422805 0.00173
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.74C>T (p.Pro25Leu) rs145310035 0.00147
NM_000426.4(LAMA2):c.1650C>T (p.Gly550=) rs899353 0.00120
NM_000426.4(LAMA2):c.255C>T (p.Ile85=) rs142083777 0.00116
NM_000426.4(LAMA2):c.6697G>A (p.Val2233Ile) rs150945378 0.00086
NM_000426.4(LAMA2):c.922G>A (p.Glu308Lys) rs146462599 0.00086
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.5531G>A (p.Arg1844His) rs150691000 0.00056
NM_000426.4(LAMA2):c.7300+10T>A rs200469923 0.00056
NM_000426.4(LAMA2):c.1645C>T (p.Pro549Ser) rs139070796 0.00052
NM_000426.4(LAMA2):c.4926A>G (p.Thr1642=) rs62421010 0.00034
NM_000426.4(LAMA2):c.903G>A (p.Ala301=) rs148655840 0.00032
NM_000426.4(LAMA2):c.5291A>G (p.Glu1764Gly) rs141950826 0.00014
NM_000426.4(LAMA2):c.9161C>A (p.Ala3054Glu) rs151049890 0.00010
NM_000426.4(LAMA2):c.9262A>G (p.Ile3088Val) rs768834542 0.00010
NM_000426.4(LAMA2):c.2736G>A (p.Ala912=) rs142671449 0.00009
NM_000426.4(LAMA2):c.8223G>A (p.Thr2741=) rs150596964 0.00009
NM_000426.4(LAMA2):c.4301C>T (p.Ser1434Leu) rs368379507 0.00006
NM_000426.4(LAMA2):c.7344T>C (p.Asn2448=) rs199931560 0.00006
NM_000426.4(LAMA2):c.4263A>G (p.Gln1421=) rs374353607 0.00005
NM_000426.4(LAMA2):c.4554C>A (p.Gly1518=) rs767497614 0.00004
NM_000426.4(LAMA2):c.8727C>T (p.Cys2909=) rs148285711 0.00004
NM_000426.4(LAMA2):c.5382A>G (p.Thr1794=) rs565429072 0.00003
NM_000426.4(LAMA2):c.5553C>T (p.Ser1851=) rs781341719 0.00003
NM_000426.4(LAMA2):c.243G>T (p.Pro81=) rs766642494 0.00002
NM_000426.4(LAMA2):c.6567C>T (p.Ala2189=) rs748650667 0.00002
NM_000426.4(LAMA2):c.7231G>A (p.Val2411Ile) rs199814707 0.00002
NM_000426.4(LAMA2):c.2286T>C (p.His762=) rs762354749 0.00001
NM_000426.4(LAMA2):c.4749C>T (p.Leu1583=) rs754850670 0.00001
NM_000426.4(LAMA2):c.5409A>G (p.Leu1803=) rs751359270 0.00001
NM_000426.4(LAMA2):c.85C>A (p.Arg29=) rs762102801 0.00001
NM_000426.4(LAMA2):c.3108C>T (p.Thr1036=)
NM_000426.4(LAMA2):c.3231C>A (p.Gly1077=) rs376529091
NM_000426.4(LAMA2):c.3432C>T (p.His1144=)
NM_000426.4(LAMA2):c.3872T>C (p.Met1291Thr)
NM_000426.4(LAMA2):c.4623T>G (p.Pro1541=)
NM_000426.4(LAMA2):c.4983C>T (p.Gly1661=)
NM_000426.4(LAMA2):c.5074G>C (p.Val1692Leu) rs567613582
NM_000426.4(LAMA2):c.5140T>C (p.Leu1714=) rs572008421
NM_000426.4(LAMA2):c.5652G>A (p.Arg1884=) rs2114694780
NM_000426.4(LAMA2):c.5961T>C (p.Asp1987=) rs761267338
NM_000426.4(LAMA2):c.6531T>C (p.Ala2177=)
NM_000426.4(LAMA2):c.7176G>A (p.Glu2392=) rs763694058
NM_000426.4(LAMA2):c.8076-31_8076-29del
NM_000426.4(LAMA2):c.8673C>A (p.Pro2891=)
NM_000426.4(LAMA2):c.8928T>A (p.Val2976=)

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