ClinVar Miner

Variants in gene GATA2 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 12
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HGVS dbSNP
NM_001145661.2(GATA2):c.*183C>T rs45598538
NM_001145661.2(GATA2):c.114G>A (p.Gln38=) rs775573177
NM_001145661.2(GATA2):c.1233G>A (p.Ala411=) rs34172218
NM_001145661.2(GATA2):c.333C>T (p.His111=) rs148554346
NM_001145661.2(GATA2):c.480C>T (p.Thr160=) rs199640729
NM_001145661.2(GATA2):c.481C>G (p.Pro161Ala) rs34799090
NM_001145661.2(GATA2):c.490G>A (p.Ala164Thr) rs2335052
NM_001145661.2(GATA2):c.564G>C (p.Thr188=) rs34870876
NM_001145661.2(GATA2):c.66C>G (p.Pro22=) rs113384352
NM_001145661.2(GATA2):c.710G>A (p.Gly237Asp) rs191501191
NM_001145661.2(GATA2):c.748C>G (p.Pro250Ala) rs78245253
NM_032638.4(GATA2):c.-276T>G rs563914744

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