List of variants reported as benign for Lymphedema, primary, with myelodysplasia; Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency by Invitae

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Total variants: 18

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HGVS	dbSNP
NM_001145661.2(GATA2):c.*183C>T	rs45598538
NM_001145661.2(GATA2):c.1018-19C>T	rs11708606
NM_001145661.2(GATA2):c.1143+203A>G	rs2713604
NM_001145661.2(GATA2):c.114G>A (p.Gln38=)	rs775573177
NM_001145661.2(GATA2):c.1173A>G (p.Glu391=)	rs145076941
NM_001145661.2(GATA2):c.1416G>A (p.Pro472=)	rs376805544
NM_001145661.2(GATA2):c.1431C>T (p.Thr477=)	rs754297885
NM_001145661.2(GATA2):c.279G>A (p.Pro93=)	rs142993548
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.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_032638.5(GATA2):c.1233G>A (p.Ala411=)	rs34172218
NM_032638.5(GATA2):c.15C>G (p.Pro5=)	rs1573858
NM_032638.5(GATA2):c.490G>A (p.Ala164Thr)	rs2335052

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