List of variants in gene AR reported as uncertain significance by PreventionGenetics, part of Exact Sciences

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_000044.6(AR):c.475G>A (p.Ala159Thr)	rs370215797	0.00014
NM_000044.6(AR):c.1370GCG[23] (p.Gly473_Glu474insGlyGlyGlyGlyGlyGly)
NM_000044.6(AR):c.1370GCG[5] (p.Gly462_Gly473del)	rs746853821
NM_000044.6(AR):c.280G>T (p.Asp94Tyr)	rs1007084818

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