List of variants in gene combination IRF2BP2, LOC129932812 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_182972.3(IRF2BP2):c.453G>C (p.Pro151=)	rs567164754	0.00057
NM_182972.3(IRF2BP2):c.225C>T (p.Ala75=)	rs758144487	0.00030
NM_182972.3(IRF2BP2):c.471G>C (p.Leu157=)	rs776503885	0.00006
NM_182972.3(IRF2BP2):c.339C>T (p.Ala113=)
NM_182972.3(IRF2BP2):c.352C>G (p.Pro118Ala)	rs148187914

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