C0039585[trait identifier] AND "GeneReviews"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 417975	NM_000044.6(AR):c.171GCA[36] (p.Gln68_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	Partial androgen insensitivity syndrome +4 more	GUncertain significance
Select item 155758	NM_000044.6(AR):c.639G>A (p.Glu213=)	AR	Single nucleotide variant (synonymous variant +1 more)	Androgen resistance syndrome +3 more	GBenign
Select item 155757	NM_000044.6:c.1363GGT[2_4]GGC[12_29]	AR	Microsatellite	Androgen resistance syndrome	GBenign

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