ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 110
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000426.4(LAMA2):c.4750G>A (p.Gly1584Ser) rs117781224 0.01941
NM_000426.4(LAMA2):c.1798G>A (p.Gly600Arg) rs36044314 0.01250
NM_000426.4(LAMA2):c.112+33371C>T rs139280910 0.00973
NM_000426.4(LAMA2):c.7431A>T (p.Arg2477Ser) rs34367843 0.00914
NM_000426.4(LAMA2):c.8548-10T>C rs113644365 0.00865
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.9211+6T>C rs201375881 0.00091
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.6506A>G (p.Asn2169Ser) rs144845618 0.00051
NM_000426.4(LAMA2):c.903G>A (p.Ala301=) rs148655840 0.00032
NM_000426.4(LAMA2):c.3582T>C (p.Ile1194=) rs137962409 0.00031
NM_000426.4(LAMA2):c.6832A>G (p.Met2278Val) rs146854942 0.00026
NM_000426.4(LAMA2):c.5291A>G (p.Glu1764Gly) rs141950826 0.00014
NM_000426.4(LAMA2):c.9001G>C (p.Val3001Leu) rs189360899 0.00013
NM_000426.4(LAMA2):c.3004G>A (p.Gly1002Ser) rs200953311 0.00011
NM_000426.4(LAMA2):c.4048C>T (p.Arg1350Ter) rs756854513 0.00010
NM_000426.4(LAMA2):c.8467C>T (p.Pro2823Ser) rs151334775 0.00010
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.3403A>C (p.Thr1135Pro) rs760558443 0.00005
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.7732C>T (p.Arg2578Ter) rs121913572 0.00004
NM_000426.4(LAMA2):c.8727C>T (p.Cys2909=) rs148285711 0.00004
NM_000426.4(LAMA2):c.2451-2A>G rs993196576 0.00003
NM_000426.4(LAMA2):c.2916T>G (p.Phe972Leu) rs763840955 0.00003
NM_000426.4(LAMA2):c.3085C>T (p.Arg1029Ter) rs145420388 0.00003
NM_000426.4(LAMA2):c.4960-17C>A rs758048596 0.00003
NM_000426.4(LAMA2):c.5553C>T (p.Ser1851=) rs781341719 0.00003
NM_000426.4(LAMA2):c.5688C>T (p.His1896=) rs573779258 0.00003
NM_000426.4(LAMA2):c.243G>T (p.Pro81=) rs766642494 0.00002
NM_000426.4(LAMA2):c.3215del (p.Cys1072fs) rs886041297 0.00002
NM_000426.4(LAMA2):c.5562+5G>C rs771046502 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.2639A>G (p.Asp880Gly) rs766536888 0.00001
NM_000426.4(LAMA2):c.277C>A (p.Pro93Thr) rs530988751 0.00001
NM_000426.4(LAMA2):c.2901C>A (p.Cys967Ter) rs121913577 0.00001
NM_000426.4(LAMA2):c.2T>C (p.Met1Thr) rs374403765 0.00001
NM_000426.4(LAMA2):c.4592C>G (p.Pro1531Arg) rs760292213 0.00001
NM_000426.4(LAMA2):c.4749C>T (p.Leu1583=) rs754850670 0.00001
NM_000426.4(LAMA2):c.5285G>A (p.Arg1762Gln) rs138296015 0.00001
NM_000426.4(LAMA2):c.5409A>G (p.Leu1803=) rs751359270 0.00001
NM_000426.4(LAMA2):c.6421G>A (p.Ala2141Thr) rs768685078 0.00001
NM_000426.4(LAMA2):c.6599G>A (p.Arg2200His) rs779326725 0.00001
NM_000426.4(LAMA2):c.6956G>A (p.Arg2319Gln) rs750013590 0.00001
NM_000426.4(LAMA2):c.85C>A (p.Arg29=) rs762102801 0.00001
GRCh37/hg19 6q22.33(chr6:129612759-129622017)x3
NM_000426.4(LAMA2):c.1027+1G>A rs1064797327
NM_000426.4(LAMA2):c.1028-6A>G rs1778989846
NM_000426.4(LAMA2):c.112+1G>C rs398123367
NM_000426.4(LAMA2):c.1240T>C (p.Cys414Arg) rs778370179
NM_000426.4(LAMA2):c.13G>T (p.Ala5Ser) rs367622987
NM_000426.4(LAMA2):c.1762del (p.Ala588fs) rs786205654
NM_000426.4(LAMA2):c.2049_2050del (p.Arg683fs) rs202247790
NM_000426.4(LAMA2):c.2059C>G (p.Gln687Glu) rs1583345100
NM_000426.4(LAMA2):c.2111A>G (p.Asn704Ser) rs1583362157
NM_000426.4(LAMA2):c.3172A>T (p.Lys1058Ter) rs1583447808
NM_000426.4(LAMA2):c.3217A>G (p.Asn1073Asp)
NM_000426.4(LAMA2):c.3231C>A (p.Gly1077=) rs376529091
NM_000426.4(LAMA2):c.3667del (p.Asp1222_Leu1223insTer) rs1774538111
NM_000426.4(LAMA2):c.3872T>C (p.Met1291Thr)
NM_000426.4(LAMA2):c.4510C>T (p.Gln1504Ter)
NM_000426.4(LAMA2):c.4623T>G (p.Pro1541=)
NM_000426.4(LAMA2):c.4649C>T (p.Pro1550Leu) rs1554278657
NM_000426.4(LAMA2):c.4717+1G>T rs1131691660
NM_000426.4(LAMA2):c.4983C>T (p.Gly1661=)
NM_000426.4(LAMA2):c.5074G>C (p.Val1692Leu) rs567613582
NM_000426.4(LAMA2):c.5195dup (p.Asn1732fs) rs747567057
NM_000426.4(LAMA2):c.5530C>A (p.Arg1844Ser) rs56173620
NM_000426.4(LAMA2):c.5530C>T (p.Arg1844Cys) rs56173620
NM_000426.4(LAMA2):c.5652G>A (p.Arg1884=) rs2114694780
NM_000426.4(LAMA2):c.5866-1G>A rs1064797040
NM_000426.4(LAMA2):c.6531T>C (p.Ala2177=)
NM_000426.4(LAMA2):c.6671T>C (p.Ile2224Thr) rs775847695
NM_000426.4(LAMA2):c.6752C>A (p.Pro2251His) rs546395293
NM_000426.4(LAMA2):c.6985_6988del (p.Thr2329fs) rs1064797328
NM_000426.4(LAMA2):c.7040G>T (p.Gly2347Val) rs529981007
NM_000426.4(LAMA2):c.7176G>A (p.Glu2392=) rs763694058
NM_000426.4(LAMA2):c.8076-3T>C
NM_000426.4(LAMA2):c.855G>T (p.Gly285=) rs1008267864
NM_000426.4(LAMA2):c.8673C>A (p.Pro2891=)
NM_000426.4(LAMA2):c.8689C>T (p.Arg2897Ter) rs750328754
NM_000426.4(LAMA2):c.9340G>A (p.Val3114Ile) rs200796753

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.