ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 53
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000426.4(LAMA2):c.7431A>T (p.Arg2477Ser) rs34367843 0.00914
NM_000426.4(LAMA2):c.4437-5T>A rs41285288 0.00557
NM_000426.4(LAMA2):c.2476C>T (p.Arg826Trp) rs118147866 0.00549
NM_000426.4(LAMA2):c.4470C>T (p.Asp1490=) rs35089085 0.00547
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.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.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.7300+10T>A rs200469923 0.00056
NM_000426.4(LAMA2):c.1645C>T (p.Pro549Ser) rs139070796 0.00052
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.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.3231C>A (p.Gly1077=) rs376529091
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.6531T>C (p.Ala2177=)
NM_000426.4(LAMA2):c.7176G>A (p.Glu2392=) rs763694058
NM_000426.4(LAMA2):c.8673C>A (p.Pro2891=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.