ClinVar Miner

List of variants in gene LAMA2 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_000426.4(LAMA2):c.4487C>T (p.Ala1496Val) rs147077184 0.00338
NM_000426.4(LAMA2):c.1621A>G (p.Ser541Gly) rs141363186 0.00175
NM_000426.4(LAMA2):c.7111T>G (p.Phe2371Val) rs150644209 0.00164
NM_000426.4(LAMA2):c.9211+6T>C rs201375881 0.00091
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.1400A>G (p.Lys467Arg) rs138162760 0.00071
NM_000426.4(LAMA2):c.3532G>A (p.Ala1178Thr) rs34505698 0.00066
NM_000426.4(LAMA2):c.7250A>G (p.His2417Arg) rs147185142 0.00053
NM_000426.4(LAMA2):c.2217G>T (p.Trp739Cys) rs192317605 0.00039
NM_000426.4(LAMA2):c.2009G>A (p.Arg670His) rs149305108 0.00034
NM_000426.4(LAMA2):c.3244C>T (p.His1082Tyr) rs146490004 0.00028
NM_000426.4(LAMA2):c.6832A>G (p.Met2278Val) rs146854942 0.00026
NM_000426.4(LAMA2):c.4010A>G (p.His1337Arg) rs139739075 0.00024
NM_000426.4(LAMA2):c.6002G>A (p.Arg2001Lys) rs151009169 0.00023
NM_000426.4(LAMA2):c.5689G>A (p.Ala1897Thr) rs200518204 0.00021
NM_000426.4(LAMA2):c.2932G>A (p.Asp978Asn) rs202050052 0.00020
NM_000426.4(LAMA2):c.5558T>G (p.Ile1853Arg) rs141911213 0.00020
NM_000426.4(LAMA2):c.7415G>T (p.Gly2472Val) rs200921233 0.00019
NM_000426.4(LAMA2):c.7088C>T (p.Thr2363Ile) rs371403343 0.00017
NM_000426.4(LAMA2):c.4675G>A (p.Gly1559Ser) rs377630412 0.00016
NM_000426.4(LAMA2):c.7985T>C (p.Val2662Ala) rs138732723 0.00016
NM_000426.4(LAMA2):c.2993G>A (p.Arg998His) rs144946631 0.00014
NM_000426.4(LAMA2):c.3628A>G (p.Ile1210Val) rs147291222 0.00014
NM_000426.4(LAMA2):c.542A>G (p.Asn181Ser) rs143664472 0.00014
NM_000426.4(LAMA2):c.2132A>G (p.Tyr711Cys) rs201122410 0.00012
NM_000426.4(LAMA2):c.4993G>A (p.Gly1665Arg) rs373997222 0.00012
NM_000426.4(LAMA2):c.6322C>T (p.Arg2108Trp) rs139824017 0.00012
NM_000426.4(LAMA2):c.1373G>A (p.Arg458Lys) rs140604077 0.00011
NM_000426.4(LAMA2):c.3004G>A (p.Gly1002Ser) rs200953311 0.00011
NM_000426.4(LAMA2):c.8147G>A (p.Arg2716His) rs142781107 0.00011
NM_000426.4(LAMA2):c.4060A>G (p.Ile1354Val) rs143674727 0.00010
NM_000426.4(LAMA2):c.623C>A (p.Pro208His) rs183890063 0.00010
NM_000426.4(LAMA2):c.4166T>C (p.Leu1389Pro) rs752934825 0.00009
NM_000426.4(LAMA2):c.5179G>C (p.Glu1727Gln) rs374201203 0.00007
NM_000426.4(LAMA2):c.6598C>T (p.Arg2200Cys) rs568648664 0.00007
NM_000426.4(LAMA2):c.6884G>A (p.Arg2295His) rs142164767 0.00006
NM_000426.4(LAMA2):c.7075C>T (p.Pro2359Ser) rs535022442 0.00006
NM_000426.4(LAMA2):c.676G>A (p.Asp226Asn) rs149654569 0.00005
NM_000426.4(LAMA2):c.2512G>A (p.Gly838Arg) rs150361703 0.00004
NM_000426.4(LAMA2):c.2831A>G (p.Gln944Arg) rs141920360 0.00004
NM_000426.4(LAMA2):c.5050G>A (p.Glu1684Lys) rs201632009 0.00004
NM_000426.4(LAMA2):c.6539A>T (p.Asp2180Val) rs567385461 0.00004
NM_000426.4(LAMA2):c.7073A>G (p.Tyr2358Cys) rs773157433 0.00004
NM_000426.4(LAMA2):c.2477G>A (p.Arg826Gln) rs759973830 0.00003
NM_000426.4(LAMA2):c.1495C>T (p.Arg499Cys) rs143626559 0.00002
NM_000426.4(LAMA2):c.358G>A (p.Glu120Lys) rs778869610 0.00002
NM_000426.4(LAMA2):c.7231G>A (p.Val2411Ile) rs199814707 0.00002
NM_000426.4(LAMA2):c.2777T>C (p.Phe926Ser) rs1789709370 0.00001
NM_000426.4(LAMA2):c.301A>G (p.Asn101Asp) rs1355569168 0.00001
NM_000426.4(LAMA2):c.3129A>T (p.Lys1043Asn) rs772541077 0.00001
NM_000426.4(LAMA2):c.3203T>C (p.Leu1068Ser) rs752736343 0.00001
NM_000426.4(LAMA2):c.4234C>T (p.Pro1412Ser) rs1775426933 0.00001
NM_000426.4(LAMA2):c.4544G>T (p.Gly1515Val) rs370406703 0.00001
NM_000426.4(LAMA2):c.7780C>T (p.Arg2594Cys) rs546988105 0.00001
NM_000426.4(LAMA2):c.8684C>G (p.Thr2895Ser) rs200705442 0.00001
NM_000426.4(LAMA2):c.1336A>G (p.Thr446Ala)
NM_000426.4(LAMA2):c.3130T>C (p.Cys1044Arg) rs2114461161
NM_000426.4(LAMA2):c.408C>G (p.Ile136Met) rs145149634
NM_000426.4(LAMA2):c.4222C>G (p.Arg1408Gly) rs780127363
NM_000426.4(LAMA2):c.437C>T (p.Ser146Phe) rs143680577
NM_000426.4(LAMA2):c.4679G>A (p.Cys1560Tyr)
NM_000426.4(LAMA2):c.5012C>G (p.Thr1671Ser) rs2114654061
NM_000426.4(LAMA2):c.5765C>T (p.Thr1922Ile)
NM_000426.4(LAMA2):c.6328A>G (p.Ile2110Val) rs531424175
NM_000426.4(LAMA2):c.643C>T (p.His215Tyr) rs2114958647
NM_000426.4(LAMA2):c.7040G>A (p.Gly2347Asp) rs529981007
NM_000426.4(LAMA2):c.7390_7391delinsTT (p.Ala2464Leu) rs1554303509
NM_000426.4(LAMA2):c.7439+6T>G rs767494596
NM_000426.4(LAMA2):c.8041G>C (p.Glu2681Gln) rs2114859864
NM_000426.4(LAMA2):c.8534G>T (p.Gly2845Val)
NM_000426.4(LAMA2):c.8918C>A (p.Thr2973Lys) rs145842163
NM_000426.4(LAMA2):c.9038A>C (p.Asp3013Ala) rs765377729
NM_000426.4(LAMA2):c.917G>A (p.Arg306His) rs1023922833
NM_000426.4(LAMA2):c.9340G>A (p.Val3114Ile) rs200796753

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