ClinVar Miner

List of variants in gene MAGI2 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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Total variants: 19
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HGVS dbSNP gnomAD frequency
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.1717C>G (p.Pro573Ala) rs145925666 0.00010
NM_012301.4(MAGI2):c.2830T>C (p.Ser944Pro) rs751956751 0.00010
NM_012301.4(MAGI2):c.1777A>G (p.Met593Val) rs745364999 0.00009
NM_012301.4(MAGI2):c.3083C>T (p.Ala1028Val) rs148526889 0.00009
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.2117C>T (p.Thr706Met) rs773722155 0.00003
NM_012301.4(MAGI2):c.1530C>T (p.Tyr510=) rs201057526 0.00002
NM_012301.4(MAGI2):c.1406C>T (p.Thr469Ile) rs770681130 0.00001
NM_012301.4(MAGI2):c.3022C>T (p.Pro1008Ser) rs764279398 0.00001
NM_012301.4(MAGI2):c.743T>A (p.Val248Glu) rs761048587 0.00001
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.3079_3096dup (p.Met1027_Pro1032dup) rs773020054
NM_012301.4(MAGI2):c.4255C>G (p.Pro1419Ala) rs1584845985

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