List of variants in gene GATA2 reported as benign for not provided

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_032638.5(GATA2):c.1143+203A>G	rs2713604	0.69604
NM_032638.5(GATA2):c.15C>G (p.Pro5=)	rs1573858	0.68160
NM_032638.5(GATA2):c.872-187T>C	rs2713602	0.61669
NM_032638.5(GATA2):c.1143+128C>T	rs2713603	0.42696
NM_032638.5(GATA2):c.1018-226T>G	rs11717152	0.23569
NM_032638.5(GATA2):c.*200C>T	rs10934857	0.22831
NM_032638.5(GATA2):c.1018-19C>T	rs11708606	0.17884
NM_032638.5(GATA2):c.490G>A (p.Ala164Thr)	rs2335052	0.17829
NM_032638.5(GATA2):c.229+127C>T	rs4577488	0.17609
NM_032638.5(GATA2):c.871+342C>T	rs72983369	0.05503
NM_032638.5(GATA2):c.564G>C (p.Thr188=)	rs34870876	0.04681
NM_032638.5(GATA2):c.1233G>A (p.Ala411=)	rs34172218	0.01909
NM_032638.5(GATA2):c.481C>G (p.Pro161Ala)	rs34799090	0.00854
NM_032638.5(GATA2):c.748C>G (p.Pro250Ala)	rs78245253	0.00309
NM_032638.5(GATA2):c.121C>G (p.Pro41Ala)	rs143590990	0.00064
NM_032638.5(GATA2):c.*100C>A
NM_032638.5(GATA2):c.1143+242G>C
NM_032638.5(GATA2):c.872-158C>A	rs2659689

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