ClinVar for MedGen (Select 865018) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 587547	NM_000044.6(AR):c.1370GCG[5] (p.Gly462_Gly473del)	AR	Microsatellite (inframe_deletion +1 more)	Androgen resistance syndrome +3 more	GUncertain significance
Select item 9828	NM_000044.6(AR):c.1826G>A (p.Arg609Lys)	AR (R609K +1 more)	Single nucleotide variant (missense variant +1 more)	Androgen insensitivity, partial, with breast cancer	GPathogenic