ClinVar Miner

List of variants in gene LAMC2 reported by GeneDx

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Gene type:
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Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_005562.3(LAMC2):c.268+14A>G rs647347 0.45636
NM_005562.3(LAMC2):c.2301-233G>A rs2296302 0.30160
NM_005562.3(LAMC2):c.404+125T>G rs875794 0.30148
NM_005562.3(LAMC2):c.798T>G (p.Gly266=) rs1047980 0.29549
NM_005562.3(LAMC2):c.1066+226G>A rs6694348 0.29534
NM_005562.3(LAMC2):c.2688G>A (p.Gln896=) rs1047981 0.29455
NM_005562.3(LAMC2):c.641-80C>T rs2296307 0.25699
NM_005562.3(LAMC2):c.954-124A>G rs2021956 0.25654
NM_005562.3(LAMC2):c.641-295_641-294insG rs34982665 0.25649
NM_005562.3(LAMC2):c.404+237C>T rs875795 0.25596
NM_005562.3(LAMC2):c.269-64C>T rs2274981 0.25583
NM_005562.3(LAMC2):c.483C>T (p.Val161=) rs1129723 0.25575
NM_005562.3(LAMC2):c.297C>T (p.Ser99=) rs2274980 0.25565
NM_005562.3(LAMC2):c.405-31T>C rs10911285 0.25565
NM_005562.3(LAMC2):c.3329-111C>A rs3768594 0.23937
NM_005562.3(LAMC2):c.2198G>C (p.Ser733Thr) rs2296303 0.16512
NM_005562.3(LAMC2):c.2457-115C>T rs3738823 0.16357
NM_005562.3(LAMC2):c.3069+144T>G rs648809 0.14367
NM_005562.3(LAMC2):c.953+37A>G rs3738824 0.12798
NM_005562.3(LAMC2):c.269-160C>T rs2274982 0.10279
NM_005562.3(LAMC2):c.2456+139G>T rs73049785 0.10078
NM_005562.3(LAMC2):c.1714+259C>T rs3768597 0.09467
NM_005562.3(LAMC2):c.371C>T (p.Thr124Met) rs11586699 0.05840
NM_005562.3(LAMC2):c.1285+166C>A rs16860609 0.05831
NM_005562.3(LAMC2):c.3069+147T>C rs2296301 0.04809
NM_005562.3(LAMC2):c.3070-96C>T rs2477437 0.04231
NM_005562.3(LAMC2):c.3367C>T (p.Leu1123=) rs587281 0.03867
NM_005562.3(LAMC2):c.1714+74G>A rs7537499 0.03748
NM_005562.3(LAMC2):c.3328+107A>G rs644673 0.03689
NM_005562.3(LAMC2):c.331G>C (p.Ala111Pro) rs12065473 0.03585
NM_005562.3(LAMC2):c.3070-157A>G rs77640423 0.03561
NM_005562.3(LAMC2):c.741C>A (p.Asp247Glu) rs2296306 0.03381
NM_005562.3(LAMC2):c.268+53A>G rs113949287 0.02506
NM_005562.3(LAMC2):c.268+39G>A rs61809149 0.02369
NM_005562.3(LAMC2):c.1285+182C>A rs73049782 0.01743
NM_005562.3(LAMC2):c.1468+219C>T rs73049783 0.01740
NM_005562.3(LAMC2):c.763+303C>T rs16860588 0.01702
NM_005562.3(LAMC2):c.269-15C>T rs12085883 0.00715
NM_005562.3(LAMC2):c.196G>A (p.Glu66Lys) rs146325169 0.00114
NM_005562.3(LAMC2):c.1350C>A (p.Tyr450Ter) rs201308300 0.00002
NM_005562.3(LAMC2):c.847T>C (p.Ser283Pro) rs763119021 0.00002
NM_005562.3(LAMC2):c.3454C>T (p.Gln1152Ter) rs1217053724 0.00001
NM_005562.3(LAMC2):c.1066+12C>A rs12092752
NM_005562.3(LAMC2):c.1286-283C>T rs12094412
NM_005562.3(LAMC2):c.1469-204A>G rs6658628
NM_005562.3(LAMC2):c.2419_2438delinsG (p.Ser807fs) rs1571538391
NM_005562.3(LAMC2):c.2457-54del rs34154823
NM_005562.3(LAMC2):c.2457-55_2457-54del rs34154823
NM_005562.3(LAMC2):c.268+250T>C rs635796
NM_005562.3(LAMC2):c.2755-336C>G rs4651151
NM_005562.3(LAMC2):c.2967G>C (p.Lys989Asn) rs1553267625
NM_005562.3(LAMC2):c.3070-89C>A rs2477436
NM_005562.3(LAMC2):c.80-31del rs10668798
NM_005562.3(LAMC2):c.80-31dup rs10668798
NM_005562.3(LAMC2):c.80-32_80-31dup rs10668798
NM_005562.3(LAMC2):c.80-33_80-31dup rs10668798

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