"Fulgent Genetics, Fulgent Genetics"[submitter] AND "LOC109504725"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1189467	NM_000044.6(AR):c.171GCA[35] (p.Gln69_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	Androgen resistance syndrome +5 more	GLikely benign
Select item 422605	NM_000044.6(AR):c.171GCA[32] (p.Gln72_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	not provided +6 more	GBenign/Likely benign
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 516217	NM_000044.6(AR):c.171GCA[14] (p.Gln72_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	Androgen resistance syndrome +6 more	GLikely benign
Select item 464798	NM_000044.6(AR):c.171GCA[22] (p.Gln80del)	AR, LOC109504725 (Q80del)	Microsatellite (inframe_deletion +1 more)	Kennedy disease +5 more	GBenign
Select item 434254	NM_000044.6(AR):c.171GCA[18] (p.Gln76_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	Hypospadias 1, X-linked +6 more	GBenign/Likely benign
Select item 402390	NM_000044.6(AR):c.173A>T (p.Gln58Leu)	AR, LOC109504725 (Q58L)	Single nucleotide variant (missense variant +1 more)	Male infertility +7 more	GConflicting classifications of pathogenicity

ClinVar