List of variants in gene IRF2BPL reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
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: 4

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HGVS	dbSNP	gnomAD frequency
NM_024496.4(IRF2BPL):c.1607G>T (p.Gly536Val)	rs745856019	0.00003
NM_024496.4(IRF2BPL):c.1066G>C (p.Glu356Gln)
NM_024496.4(IRF2BPL):c.2028C>G (p.Asn676Lys)
NM_024496.4(IRF2BPL):c.754G>A (p.Val252Met)

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