C0039585[trait identifier] AND "Labcorp Genetics (formerly Invitae), L - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1344508	NM_003504.5(CDC45):c.1357G>A (p.Gly453Ser)	CDC45 (G407S +3 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1470535	NM_000044.6(AR):c.1A>T (p.Met1Leu)	AR (M1L)	Single nucleotide variant (missense variant +2 more)	Androgen resistance syndrome +1 more	GPathogenic
Select item 852163	NM_000044.6(AR):c.5A>G (p.Glu2Gly)	AR (E2G)	Single nucleotide variant (missense variant +1 more)	Kennedy disease +1 more	GUncertain significance
Select item 1488550	NM_000044.6(AR):c.7G>A (p.Val3Met)	AR (V3M)	Single nucleotide variant (missense variant +1 more)	Ovarian cancer +5 more	GConflicting classifications of pathogenicity
Select item 2933125	NM_000044.6(AR):c.39G>A (p.Arg13=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GBenign
Select item 2934997	NM_000044.6(AR):c.45G>T (p.Pro15=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2930877	NM_000044.6(AR):c.45G>A (p.Pro15=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GBenign
Select item 2923962	NM_000044.6(AR):c.51G>T (p.Lys17Asn)	AR (K17N)	Single nucleotide variant (missense variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2938203	NM_000044.6(AR):c.87C>T (p.Ser29=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2946522	NM_000044.6(AR):c.119G>A (p.Arg40Lys)	AR (R40K)	Single nucleotide variant (missense variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 733466	NM_000044.6(AR):c.134C>G (p.Ala45Gly)	AR (A45G)	Single nucleotide variant (missense variant +1 more)	Androgen resistance syndrome +1 more	GLikely benign
Select item 2929009	NM_000044.6(AR):c.150C>T (p.Pro50=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 958035	NM_000044.6(AR):c.161TGC[5] (p.Leu57dup)	AR	Microsatellite (inframe_insertion +1 more)	Malignant tumor of prostate +3 more	GConflicting classifications of pathogenicity
Select item 807734	NM_000044.6(AR):c.161TGC[3] (p.Leu57del)	AR (L57del)	Microsatellite (inframe_deletion +1 more)	Kennedy disease +2 more	GLikely benign
Select item 2946727	NM_000044.6(AR):c.170AGC[7] (p.Leu56_Leu57insGlnGlnGlnGlnGlnGlnGln)	AR	Microsatellite (inframe_insertion +2 more)	Kennedy disease +1 more	GBenign
Select item 1428356	NM_000044.6(AR):c.170AGC[8] (p.Leu56_Leu57insGlnGlnGlnGlnGlnGlnGlnGln)	AR	Microsatellite (inframe_insertion +1 more)	Kennedy disease +1 more	GUncertain significance
Select item 2034843	NM_000044.6(AR):c.172_173insTGCAGCAGCAGCAGC (p.Leu57_Gln58insLeuGlnGlnGlnGln)	AR, LOC109504725	Insertion (inframe_insertion +1 more)	Androgen resistance syndrome +1 more	GUncertain significance
Select item 1403739	NM_000044.6(AR):c.172_173insTGCAGCAGCAGCAGCAGCAGC (p.Leu57_Gln58insLeuGlnGlnGlnGlnGlnGln)	AR, LOC109504725	Insertion (inframe_insertion +1 more)	Androgen resistance syndrome +1 more	GUncertain significance
Select item 1168151	NM_000044.6(AR):c.171GCA[27] (p.Gln77_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	not provided +2 more	GBenign
Select item 1049223	NM_000044.6(AR):c.170T>A (p.Leu57Gln)	AR (L57Q)	Single nucleotide variant (missense variant +1 more)	Ovarian cancer +4 more	GBenign/Likely benign
Select item 507868	NM_000044.6(AR):c.171GCA[30] (p.Gln74_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	Androgen resistance syndrome +2 more	GBenign/Likely benign
Select item 464795	NM_000044.6(AR):c.171GCA[28] (p.Gln76_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	not provided +3 more	GBenign
Select item 464794	NM_000044.6(AR):c.171GCA[31] (p.Gln73_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	not specified +2 more	GBenign/Likely benign
Select item 464788	NM_000044.6(AR):c.172_173insTGCAGCAGC (p.Leu57_Gln58insLeuGlnGln)	AR, LOC109504725	Insertion (inframe_insertion +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 434257	NM_000044.6(AR):c.171GCA[24] (p.Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	Androgen resistance syndrome +3 more	GBenign/Likely benign
Select item 422605	NM_000044.6(AR):c.171GCA[32] (p.Gln72_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	Inborn genetic diseases +6 more	GBenign/Likely benign
Select item 290422	NM_000044.6(AR):c.171GCA[25] (p.Gln79_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	Kennedy disease +4 more	GBenign
Select item 1556388	NM_000044.6(AR):c.171GCA[11] (p.Gln69_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	Androgen resistance syndrome +1 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 1166167	NM_000044.6(AR):c.171GCA[13] (p.Gln71_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	Androgen resistance syndrome +2 more	GBenign/Likely benign
Select item 533380	NM_000044.6(AR):c.171GCA[15] (p.Gln73_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	not provided +2 more	GBenign/Likely benign
Select item 464796	NM_000044.6(AR):c.171GCA[19] (p.Gln77_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	Androgen resistance syndrome +2 more	GBenign
Select item 434262	NM_000044.6(AR):c.171GCA[16] (p.Gln74_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	not specified +3 more	GBenign/Likely benign
Select item 434254	NM_000044.6(AR):c.171GCA[18] (p.Gln76_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	Androgen resistance syndrome +6 more	GBenign/Likely benign
Select item 418806	NM_000044.6(AR):c.171GCA[17] (p.Gln75_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	Androgen resistance syndrome +3 more	GBenign/Likely benign
Select item 210223	NM_000044.6(AR):c.171GCA[20] (p.Gln78_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	not provided +3 more	GBenign/Likely benign
Select item 643319	NM_000044.6(AR):c.174_175insTAG (p.Gln59Ter)	AR, LOC109504725 (Q59*)	Insertion (nonsense +1 more)	Androgen resistance syndrome +1 more	GPathogenic
Select item 846244	NM_000044.6(AR):c.183_184insTAG (p.Gln62Ter)	AR, LOC109504725 (Q62*)	Insertion (nonsense +1 more)	Androgen resistance syndrome +1 more	GPathogenic
Select item 2949018	NM_000044.6(AR):c.187C>T (p.Gln63Ter)	AR, LOC109504725 (Q63*)	Single nucleotide variant (nonsense +1 more)	Kennedy disease +1 more	GPathogenic
Select item 931831	NM_000044.6(AR):c.188A>T (p.Gln63Leu)	AR, LOC109504725 (Q63L)	Single nucleotide variant (missense variant +1 more)	Androgen resistance syndrome +3 more	GUncertain significance
Select item 2942759	NM_000044.6(AR):c.190C>T (p.Gln64Ter)	AR, LOC109504725 (Q64*)	Single nucleotide variant (nonsense +1 more)	Androgen resistance syndrome +1 more	GPathogenic
Select item 581270	NM_000044.6(AR):c.195_199delinsTT (p.Gln65_Gln67delinsHisTer)	AR, LOC109504725	Indel (nonsense +1 more)	Kennedy disease +1 more	GPathogenic
Select item 2947939	NM_000044.6(AR):c.201G>A (p.Gln67=)	AR, LOC109504725	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2937166	NM_000044.6(AR):c.222G>A (p.Gln74=)	AR, LOC109504725	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2951291	NM_000044.6(AR):c.239_240insGCAGCAGCAGTAGCAGCAGCAGCAGCA (p.Gln80_Glu81insGlnGlnGlnTer)	AR, LOC109504725	Microsatellite (nonsense +3 more)	Kennedy disease +1 more	GPathogenic
Select item 2924188	NM_000044.6(AR):c.234G>A (p.Gln78=)	AR, LOC109504725	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 937145	NM_000044.6(AR):c.239_240insGCAGCAGC (p.Glu81fs)	AR, LOC109504725 (E81fs)	Insertion (frameshift variant +1 more)	Kennedy disease +1 more	GPathogenic
Select item 2066510	NM_000044.6(AR):c.240A>G (p.Gln80=)	AR, LOC109504725	Single nucleotide variant (synonymous variant +1 more)	Androgen resistance syndrome +1 more	GLikely benign
Select item 2150456	NM_000044.6(AR):c.246T>C (p.Thr82=)	AR, LOC109504725	Single nucleotide variant (synonymous variant +1 more)	Androgen resistance syndrome +1 more	GLikely benign
Select item 1629823	NM_000044.6(AR):c.256CAG[7] (p.Gln91dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2922422	NM_000044.6(AR):c.261G>A (p.Gln87=)	AR, LOC109504725	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 458365	NM_000044.6(AR):c.268C>T (p.Gln90Ter)	AR, LOC109504725 (Q90*)	Single nucleotide variant (nonsense +1 more)	Kennedy disease +1 more	GPathogenic
Select item 2950489	NM_000044.6(AR):c.270G>T (p.Gln90His)	AR, LOC109504725 (Q90H)	Single nucleotide variant (missense variant +1 more)	Kennedy disease +1 more	GBenign
Select item 575053	NM_000044.6(AR):c.271C>T (p.Gln91Ter)	AR, LOC109504725 (Q91*)	Single nucleotide variant (nonsense +1 more)	Androgen resistance syndrome +1 more	GPathogenic
Select item 2923339	NM_000044.6(AR):c.273G>A (p.Gln91=)	AR, LOC109504725	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2945090	NM_000044.6(AR):c.291C>T (p.Pro97=)	AR	Single nucleotide variant (synonymous variant +1 more)	Androgen resistance syndrome +1 more	GLikely benign
Select item 464802	NM_000044.6(AR):c.292C>T (p.Gln98Ter)	AR (Q98*)	Single nucleotide variant (nonsense +1 more)	Androgen resistance syndrome +1 more	GPathogenic
Select item 2943300	NM_000044.6(AR):c.300T>C (p.His100=)	AR	Single nucleotide variant (synonymous variant +1 more)	Androgen resistance syndrome +1 more	GLikely benign
Select item 2930876	NM_000044.6(AR):c.302G>A (p.Arg101His)	AR (R101H)	Single nucleotide variant (missense variant +1 more)	Kennedy disease +1 more	GBenign
Select item 2001392	NM_000044.6(AR):c.304A>T (p.Arg102Ter)	AR (R102*)	Single nucleotide variant (nonsense +1 more)	Kennedy disease +1 more	GPathogenic
Select item 2934819	NM_000044.6(AR):c.312C>T (p.Pro104=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2927557	NM_000044.6(AR):c.312C>G (p.Pro104=)	AR	Single nucleotide variant (5 prime UTR variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 458367	NM_000044.6(AR):c.321C>A (p.Tyr107Ter)	AR (Y107*)	Single nucleotide variant (nonsense +1 more)	Kennedy disease +1 more	GPathogenic
Select item 1168650	NM_000044.6(AR):c.324G>C (p.Leu108=)	AR	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GBenign/Likely benign
Select item 2952522	NM_000044.6(AR):c.344_345insCAGATGAGGAACAGCA (p.Gln115delinsHisArgTer)	AR	Insertion (nonsense +2 more)	Kennedy disease +1 more	GPathogenic
Select item 2925098	NM_000044.6(AR):c.333T>C (p.Asp111=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2929313	NM_000044.6(AR):c.357G>A (p.Pro119=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 1421027	NM_000044.6(AR):c.358C>T (p.Gln120Ter)	AR (Q120*)	Single nucleotide variant (nonsense +1 more)	Kennedy disease +1 more	GPathogenic
Select item 2941921	NM_000044.6(AR):c.360G>A (p.Gln120=)	AR	Single nucleotide variant (synonymous variant +1 more)	Androgen resistance syndrome +1 more	GLikely benign
Select item 2946383	NM_000044.6(AR):c.363G>A (p.Ser121=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2949106	NM_000044.6(AR):c.381C>G (p.Pro127=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2951546	NM_000044.6(AR):c.384G>A (p.Glu128=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2931756	NM_000044.6(AR):c.393C>T (p.Cys131=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2923796	NM_000044.6(AR):c.396C>T (p.Val132=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2936647	NM_000044.6(AR):c.414C>G (p.Ala138=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GBenign
Select item 2926314	NM_000044.6(AR):c.414C>T (p.Ala138=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2937102	NM_000044.6(AR):c.420C>G (p.Ala140=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2688588	NM_000044.6(AR):c.458C>T (p.Pro153Leu)	AR (P153L)	Single nucleotide variant (missense variant +1 more)	Androgen resistance syndrome +2 more	GConflicting classifications of pathogenicity
Select item 2942475	NM_000044.6(AR):c.459G>C (p.Pro153=)	AR	Single nucleotide variant (synonymous variant +1 more)	Androgen resistance syndrome +1 more	GLikely benign
Select item 2938773	NM_000044.6(AR):c.459G>A (p.Pro153=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2953240	NM_000044.6(AR):c.462C>T (p.Asp154=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GBenign
Select item 852260	NM_000044.6(AR):c.463G>T (p.Glu155Ter)	AR (E155*)	Single nucleotide variant (nonsense +1 more)	Kennedy disease +1 more	GPathogenic
Select item 492777	NM_000044.6(AR):c.475G>A (p.Ala159Thr)	AR (A159T)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 2927052	NM_000044.6(AR):c.496C>T (p.Leu166=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2945051	NM_000044.6(AR):c.510T>C (p.Thr170=)	AR	Single nucleotide variant (synonymous variant +1 more)	Androgen resistance syndrome +1 more	GLikely benign
Select item 2946588	NM_000044.6(AR):c.519C>G (p.Gly173=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GBenign
Select item 804018	NM_000044.6(AR):c.528C>A (p.Ser176Arg)	AR (S176R)	Single nucleotide variant (missense variant +1 more)	Kennedy disease +5 more	GBenign/Likely benign
Select item 2930006	NM_000044.6(AR):c.534C>T (p.Ser178=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2947606	NM_000044.6(AR):c.546dup (p.Asp183fs)	AR (D183fs)	Duplication (frameshift variant +1 more)	Kennedy disease +1 more	GPathogenic
Select item 2922012	NM_000044.6(AR):c.559G>T (p.Glu187Ter)	AR (E187*)	Single nucleotide variant (nonsense +1 more)	Kennedy disease +1 more	GPathogenic
Select item 2946611	NM_000044.6(AR):c.593A>T (p.Gln198Leu)	AR (Q198L)	Single nucleotide variant (missense variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2950979	NM_000044.6(AR):c.597G>A (p.Gln199=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2925020	NM_000044.6(AR):c.606A>C (p.Val202=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2932891	NM_000044.6(AR):c.609C>A (p.Ser203=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GBenign
Select item 2926926	NM_000044.6(AR):c.609C>G (p.Ser203=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2946057	NM_000044.6(AR):c.621C>G (p.Ser207Arg)	AR (S207R)	Single nucleotide variant (missense variant +1 more)	Kennedy disease +1 more	GBenign
Select item 2939784	NM_000044.6(AR):c.627G>T (p.Gly209=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely benign
Select item 2929095	NM_000044.6(AR):c.633G>C (p.Ala211=)	AR	Single nucleotide variant (synonymous variant +1 more)	Kennedy disease +1 more	GLikely 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 155758	NM_000044.6(AR):c.639G>A (p.Glu213=)	AR	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GBenign

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