List of variants in gene SETX reported as benign for Amyotrophic lateral sclerosis type 4

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 60

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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.4225A>T (p.Asn1409Tyr)	rs373375060
NM_015046.7(SETX):c.4273A>G (p.Lys1425Glu)	rs534886444
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.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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