List of variants in gene IRF2BP2 reported as uncertain significance for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_182972.3(IRF2BP2):c.1330G>A (p.Ala444Thr)	rs766802305	0.00011
NM_182972.3(IRF2BP2):c.1180A>C (p.Thr394Pro)	rs138385624	0.00006
NM_182972.3(IRF2BP2):c.189C>A (p.His63Gln)	rs754511640	0.00003
NM_182972.3(IRF2BP2):c.1520C>T (p.Thr507Ile)
NM_182972.3(IRF2BP2):c.1606C>T (p.Gln536Ter)
NM_182972.3(IRF2BP2):c.1727C>T (p.Ala576Val)
NM_182972.3(IRF2BP2):c.1760C>T (p.Ser587Leu)
NM_182972.3(IRF2BP2):c.535C>G (p.Arg179Gly)	rs1367122613

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