ClinVar Miner

List of variants in gene GATA2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_032638.5(GATA2):c.66C>G (p.Pro22=) rs113384352 0.00264
NM_032638.5(GATA2):c.333C>T (p.His111=) rs148554346 0.00228
NM_032638.5(GATA2):c.1173A>G (p.Glu391=) rs145076941 0.00041
NM_032638.5(GATA2):c.729C>T (p.His243=) rs369673069 0.00016
NM_032638.5(GATA2):c.445G>A (p.Gly149Arg) rs753645971 0.00009
NM_032638.5(GATA2):c.978T>C (p.Asn326=) rs769794900 0.00008
NM_032638.5(GATA2):c.189C>T (p.Pro63=) rs763735447 0.00007
NM_032638.5(GATA2):c.213C>T (p.Ser71=) rs759513417 0.00005
NM_032638.5(GATA2):c.1143+9G>A rs533617078 0.00004
NM_032638.5(GATA2):c.1347C>A (p.Ser449=) rs150052821 0.00003
NM_032638.5(GATA2):c.480C>T (p.Thr160=) rs199640729 0.00003
NM_032638.5(GATA2):c.1017+8C>T rs200848213 0.00002
NM_032638.5(GATA2):c.927C>T (p.Asp309=) rs750077677 0.00002
NM_032638.5(GATA2):c.1020G>A (p.Ser340=) rs370166358 0.00001
NM_032638.5(GATA2):c.1038C>T (p.Gly346=) rs1175250743 0.00001
NM_032638.5(GATA2):c.1143+13C>T rs112111696 0.00001
NM_032638.5(GATA2):c.753C>T (p.Ser251=) rs1450460950 0.00001
NM_032638.5(GATA2):c.-4G>T
NM_032638.5(GATA2):c.1035C>G (p.Ala345=) rs371599112
NM_032638.5(GATA2):c.1194G>A (p.Arg398=)
NM_032638.5(GATA2):c.57G>T (p.Ala19=) rs2107673691
NM_032638.5(GATA2):c.849C>T (p.Arg283=)
NM_032638.5(GATA2):c.872-5T>C rs886038417

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