ClinVar Miner

List of variants in gene LAMA2 reported as uncertain significance by GeneDx

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Total variants: 59
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HGVS dbSNP
NM_000426.3(LAMA2):c.1373G>A (p.Arg458Lys) rs140604077
NM_000426.3(LAMA2):c.1558T>A (p.Cys520Ser) rs886061046
NM_000426.3(LAMA2):c.1609-41_1609-7=
NM_000426.3(LAMA2):c.1670A>C (p.Gln557Pro) rs1333451961
NM_000426.3(LAMA2):c.1792G>A (p.Val598Ile) rs753232836
NM_000426.3(LAMA2):c.1816A>G (p.Ile606Val) rs113022759
NM_000426.3(LAMA2):c.2054T>C (p.Leu685Pro) rs746641607
NM_000426.3(LAMA2):c.2084A>T (p.Asp695Val) rs762272518
NM_000426.3(LAMA2):c.2288C>T (p.Ala763Val) rs141521127
NM_000426.3(LAMA2):c.2382C>T (p.Gly794=) rs147744763
NM_000426.3(LAMA2):c.2462C>T (p.Thr821Met) rs117422805
NM_000426.3(LAMA2):c.2564C>G (p.Pro855Arg) rs754714449
NM_000426.3(LAMA2):c.2767G>A (p.Gly923Ser) rs144492513
NM_000426.3(LAMA2):c.2780C>T (p.Ser927Phe) rs1085307732
NM_000426.3(LAMA2):c.2932G>A (p.Asp978Asn) rs202050052
NM_000426.3(LAMA2):c.3154A>G (p.Ser1052Gly) rs149165006
NM_000426.3(LAMA2):c.3244C>T (p.His1082Tyr) rs146490004
NM_000426.3(LAMA2):c.3461G>T (p.Gly1154Val) rs922954882
NM_000426.3(LAMA2):c.3532G>A (p.Ala1178Thr) rs34505698
NM_000426.3(LAMA2):c.3850G>C (p.Ala1284Pro) rs1085307846
NM_000426.3(LAMA2):c.4060A>G (p.Ile1354Val) rs143674727
NM_000426.3(LAMA2):c.4349G>A (p.Arg1450Gln) rs148905630
NM_000426.3(LAMA2):c.437C>T (p.Ser146Phe) rs143680577
NM_000426.3(LAMA2):c.4471G>A (p.Asp1491Asn) rs375640462
NM_000426.3(LAMA2):c.4646G>A (p.Arg1549Gln) rs778508100
NM_000426.3(LAMA2):c.4657A>G (p.Thr1553Ala) rs1450772080
NM_000426.3(LAMA2):c.479A>G (p.Asp160Gly) rs147398243
NM_000426.3(LAMA2):c.4960-17C>A rs758048596
NM_000426.3(LAMA2):c.518A>T (p.Asp173Val) rs767671585
NM_000426.3(LAMA2):c.525G>C (p.Glu175Asp) rs1554217596
NM_000426.3(LAMA2):c.5291A>G (p.Glu1764Gly) rs141950826
NM_000426.3(LAMA2):c.5530C>T (p.Arg1844Cys) rs56173620
NM_000426.3(LAMA2):c.5598G>T (p.Met1866Ile) rs1554289926
NM_000426.3(LAMA2):c.5833G>A (p.Ala1945Thr) rs3828736
NM_000426.3(LAMA2):c.5978A>G (p.Asp1993Gly) rs752249871
NM_000426.3(LAMA2):c.6002G>A (p.Arg2001Lys) rs151009169
NM_000426.3(LAMA2):c.6047T>C (p.Leu2016Ser) rs773309064
NM_000426.3(LAMA2):c.6128A>G (p.Gln2043Arg) rs144155507
NM_000426.3(LAMA2):c.6274+5G>T rs367765202
NM_000426.3(LAMA2):c.6539A>T (p.Asp2180Val) rs567385461
NM_000426.3(LAMA2):c.665G>C (p.Arg222Thr) rs1267371641
NM_000426.3(LAMA2):c.6708-3A>C rs112637707
NM_000426.3(LAMA2):c.670A>G (p.Ser224Gly) rs1085307718
NM_000426.3(LAMA2):c.6832A>G (p.Met2278Val) rs146854942
NM_000426.3(LAMA2):c.7111T>G (p.Phe2371Val) rs150644209
NM_000426.3(LAMA2):c.7112T>G (p.Phe2371Cys) rs201274841
NM_000426.3(LAMA2):c.7250A>G (p.His2417Arg) rs147185142
NM_000426.3(LAMA2):c.7390G>T (p.Ala2464Ser) rs1131691621
NM_000426.3(LAMA2):c.8076-7C>G rs555377928
NM_000426.3(LAMA2):c.848T>C (p.Val283Ala) rs376917587
NM_000426.3(LAMA2):c.8690G>A (p.Arg2897Gln) rs201696115
NM_000426.3(LAMA2):c.8842G>A (p.Gly2948Ser) rs143638361
NM_000426.3(LAMA2):c.8918C>T (p.Thr2973Met) rs145842163
NM_000426.3(LAMA2):c.9001G>C (p.Val3001Leu) rs189360899
NM_000426.3(LAMA2):c.9145C>G (p.Gln3049Glu) rs146525742
NM_000426.3(LAMA2):c.917G>A (p.Arg306His) rs1023922833
NM_000426.3(LAMA2):c.9253C>T rs121913571
NM_000426.3(LAMA2):c.9269_9283dup (p.Lys3095_Gly3096insThrLeuLysLeuThr) rs1554321191
NM_000426.3(LAMA2):c.946G>A (p.Asp316Asn) rs141340479

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