ClinVar Miner

List of variants in gene MAGI2 reported as uncertain significance by Eurofins NTD LLC (GA)

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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_012301.4(MAGI2):c.2142G>A (p.Pro714=) rs144574076 0.00156
NM_012301.4(MAGI2):c.2454C>T (p.Arg818=) rs148580718 0.00081
NM_012301.4(MAGI2):c.3706+5G>A rs188293910 0.00060
NM_012301.4(MAGI2):c.2131C>A (p.Pro711Thr) rs144078604 0.00031
NM_012301.4(MAGI2):c.411G>A (p.Thr137=) rs149568072 0.00024
NM_012301.4(MAGI2):c.2660G>A (p.Arg887His) rs200068841 0.00014
NM_012301.4(MAGI2):c.3739G>A (p.Ala1247Thr) rs555798505 0.00014
NM_012301.4(MAGI2):c.1861G>A (p.Asp621Asn) rs762159792 0.00010
NM_012301.4(MAGI2):c.2830T>C (p.Ser944Pro) rs751956751 0.00010
NM_012301.4(MAGI2):c.1737C>T (p.Asp579=) rs142555732 0.00009
NM_012301.4(MAGI2):c.3083C>T (p.Ala1028Val) rs148526889 0.00009
NM_012301.4(MAGI2):c.2133G>A (p.Pro711=) rs765541438 0.00006
NM_012301.4(MAGI2):c.3707-10C>T rs769323415 0.00006
NM_012301.4(MAGI2):c.1523G>A (p.Arg508His) rs370977895 0.00004
NM_012301.4(MAGI2):c.1977T>C (p.His659=) rs142064426 0.00004
NM_012301.4(MAGI2):c.2012T>C (p.Ile671Thr) rs780041985 0.00004
NM_012301.4(MAGI2):c.817C>G (p.Pro273Ala) rs202222389 0.00004
NM_012301.4(MAGI2):c.927A>T (p.Glu309Asp) rs773358292 0.00004
NM_012301.4(MAGI2):c.1530C>T (p.Tyr510=) rs201057526 0.00002
NM_012301.4(MAGI2):c.3381C>T (p.Pro1127=) rs144084071 0.00002
NM_012301.4(MAGI2):c.644G>A (p.Arg215Gln) rs886043298 0.00002
NM_012301.4(MAGI2):c.878C>T (p.Thr293Ile) rs587780389 0.00002
NM_012301.4(MAGI2):c.11G>T (p.Ser4Ile) rs766971610 0.00001
NM_012301.4(MAGI2):c.1406C>T (p.Thr469Ile) rs770681130 0.00001
NM_012301.4(MAGI2):c.1954C>A (p.Gln652Lys) rs780242449 0.00001
NM_012301.4(MAGI2):c.2160A>T (p.Pro720=) rs1186653469 0.00001
NM_012301.4(MAGI2):c.1391A>G (p.Asp464Gly) rs759295052
NM_012301.4(MAGI2):c.2384G>A (p.Gly795Glu) rs398124256
NM_012301.4(MAGI2):c.2723C>G (p.Pro908Arg) rs150080418
NM_012301.4(MAGI2):c.2958G>T (p.Met986Ile) rs779365635
NM_012301.4(MAGI2):c.3450G>A (p.Met1150Ile) rs1563153542
NM_012301.4(MAGI2):c.3798T>C (p.Ser1266=) rs752850710
NM_012301.4(MAGI2):c.507T>C (p.Ser169=) rs1192847489

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