List of variants in gene PUF60 reported as likely benign for 8q24.3 microdeletion syndrome

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_078480.3(PUF60):c.1254G>A (p.Glu418=)	rs117178721	0.00062
NM_078480.3(PUF60):c.116C>T (p.Thr39Ile)
NM_078480.3(PUF60):c.60GGC[6] (p.Ala25dup)	rs540307276

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