List of variants in gene combination IRF2BPL, LOC107984638 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_024496.4(IRF2BPL):c.90C>T (p.Phe30=)	rs371546648	0.00009
NM_024496.4(IRF2BPL):c.46C>T (p.Leu16=)	rs761071985	0.00002
NM_024496.4(IRF2BPL):c.79A>C (p.Ile27Leu)	rs770030016	0.00002
NM_024496.4(IRF2BPL):c.174G>A (p.Lys58=)
NM_024496.4(IRF2BPL):c.48G>C (p.Leu16=)	rs1182800711
NM_024496.4(IRF2BPL):c.6G>C (p.Ser2=)	rs145125439

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