List of variants in gene combination IRF2BP2, LOC129932812 reported as benign 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_182972.3(IRF2BP2):c.232T>C (p.Ser78Pro)	rs7545855	0.74265
NM_182972.3(IRF2BP2):c.352C>T (p.Pro118Ser)	rs148187914	0.02203
NM_182972.3(IRF2BP2):c.281AGC[6] (p.Gln98dup)	rs371994015

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