ClinVar Miner

List of variants in gene SETX reported as benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 59
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HGVS dbSNP
NM_015046.7(SETX):c.*1052T>A rs12349210
NM_015046.7(SETX):c.*1148T>G
NM_015046.7(SETX):c.*1224G>C rs10491906
NM_015046.7(SETX):c.*1288T>C rs72765812
NM_015046.7(SETX):c.*1365G>T rs7875801
NM_015046.7(SETX):c.*1368G>A rs7025
NM_015046.7(SETX):c.*1370G>C
NM_015046.7(SETX):c.*168C>T
NM_015046.7(SETX):c.*1700G>T rs75682594
NM_015046.7(SETX):c.*1803G>A
NM_015046.7(SETX):c.*2190A>G
NM_015046.7(SETX):c.*2232T>C rs545456048
NM_015046.7(SETX):c.*2262A>G rs997784
NM_015046.7(SETX):c.*2506T>C rs73545065
NM_015046.7(SETX):c.*319C>T rs1056912
NM_015046.7(SETX):c.*351G>T rs117409290
NM_015046.7(SETX):c.*475A>C
NM_015046.7(SETX):c.*548A>T rs139883935
NM_015046.7(SETX):c.*561A>C rs73661150
NM_015046.7(SETX):c.*562C>A rs11787894
NM_015046.7(SETX):c.*626C>T rs11795382
NM_015046.7(SETX):c.*717T>C rs17148857
NM_015046.7(SETX):c.*849G>T rs74975459
NM_015046.7(SETX):c.*905A>G rs58327306
NM_015046.7(SETX):c.-124C>T
NM_015046.7(SETX):c.-70T>C
NM_015046.7(SETX):c.1077T>C (p.Tyr359=) rs9411449
NM_015046.7(SETX):c.1693T>C (p.Phe565Leu) rs143982186
NM_015046.7(SETX):c.1880T>C (p.Met627Thr) rs199707503
NM_015046.7(SETX):c.1979C>G (p.Ala660Gly) rs882709
NM_015046.7(SETX):c.2216G>A (p.Gly739Glu) rs36024203
NM_015046.7(SETX):c.2469C>G (p.Phe823Leu) rs141163823
NM_015046.7(SETX):c.2975A>G (p.Lys992Arg) rs61742937
NM_015046.7(SETX):c.3103A>G (p.Lys1035Glu) rs117229601
NM_015046.7(SETX):c.3147C>T (p.His1049=) rs3739921
NM_015046.7(SETX):c.3182C>T (p.Pro1061Leu) rs12352982
NM_015046.7(SETX):c.3310C>G (p.Gln1104Glu) rs113831637
NM_015046.7(SETX):c.3455T>G (p.Phe1152Cys) rs3739922
NM_015046.7(SETX):c.3576T>G (p.Asp1192Glu) rs1185193
NM_015046.7(SETX):c.3663G>C (p.Lys1221Asn) rs12344006
NM_015046.7(SETX):c.3754G>A (p.Gly1252Arg) rs1183768
NM_015046.7(SETX):c.3992C>T (p.Pro1331Leu) rs11243731
NM_015046.7(SETX):c.4156A>G (p.Ile1386Val) rs543573
NM_015046.7(SETX):c.4204A>T (p.Thr1402Ser) rs150421712
NM_015046.7(SETX):c.472T>G (p.Leu158Val) rs145438764
NM_015046.7(SETX):c.4755T>G (p.Pro1585=) rs151237267
NM_015046.7(SETX):c.5563A>G (p.Thr1855Ala) rs2296871
NM_015046.7(SETX):c.5781+12dup rs3831154
NM_015046.7(SETX):c.5811T>C (p.Asp1937=) rs2296869
NM_015046.7(SETX):c.59G>A (p.Arg20His) rs79740039
NM_015046.7(SETX):c.6106+14G>A rs73661157
NM_015046.7(SETX):c.6507G>A (p.Gly2169=) rs34073320
NM_015046.7(SETX):c.6935+8T>C rs17148873
NM_015046.7(SETX):c.7114G>A (p.Asp2372Asn) rs150673589
NM_015046.7(SETX):c.7371T>C (p.His2457=) rs113071480
NM_015046.7(SETX):c.7724C>T (p.Pro2575Leu) rs34000644
NM_015046.7(SETX):c.7759A>G (p.Ile2587Val) rs1056899
NM_015046.7(SETX):c.7834A>G (p.Ser2612Gly) rs3739927
NM_015046.7(SETX):c.7914C>T (p.Phe2638=) rs80296256

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