"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1285161	NM_000044.6(AR):c.171GCA[29] (p.Gln75_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	not provided	GBenign
Select item 464797	NM_000044.6(AR):c.171GCA[26] (p.Gln78_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	not provided	GBenign
Select item 434257	NM_000044.6(AR):c.171GCA[24] (p.Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	not specified +3 more	GBenign/Likely benign
Select item 290422	NM_000044.6(AR):c.171GCA[25] (p.Gln79_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	not provided +4 more	GBenign
Select item 1276845	NM_000044.6(AR):c.171GCA[21] (p.Gln79_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	not provided +2 more	GBenign
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 464796	NM_000044.6(AR):c.171GCA[19] (p.Gln77_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	Kennedy disease +2 more	GBenign
Select item 210223	NM_000044.6(AR):c.171GCA[20] (p.Gln78_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	not specified +3 more	GBenign/Likely benign
Select item 533381	NM_000044.6(AR):c.636G>A (p.Arg212=)	AR	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign
Select item 216890	NM_000044.6(AR):c.1174C>T (p.Pro392Ser)	AR (P392S)	Single nucleotide variant (missense variant +1 more)	Androgen resistance syndrome +4 more	GConflicting classifications of pathogenicity
Select item 804019	NM_000044.6(AR):c.1424C>T (p.Ala475Val)	AR (A475V)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 9861	NM_000044.6(AR):c.1937C>A (p.Ala646Asp)	AR (A114D +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity