ClinVar Miner

List of variants in gene SETX reported as benign by PreventionGenetics,PreventionGenetics

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Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_015046.7(SETX):c.1077T>C (p.Tyr359=) rs9411449
NM_015046.7(SETX):c.1979C>G (p.Ala660Gly) rs882709
NM_015046.7(SETX):c.2975A>G (p.Lys992Arg) rs61742937
NM_015046.7(SETX):c.3147C>T (p.His1049=) rs3739921
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.3754G>A (p.Gly1252Arg) rs1183768
NM_015046.7(SETX):c.4156A>G (p.Ile1386Val) rs543573
NM_015046.7(SETX):c.4755T>G (p.Pro1585=) rs151237267
NM_015046.7(SETX):c.498+20G>A rs73659013
NM_015046.7(SETX):c.498+30T>C rs11790312
NM_015046.7(SETX):c.5374+16C>T rs2296872
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.6106+14G>A rs73661157
NM_015046.7(SETX):c.6507G>A (p.Gly2169=) rs34073320
NM_015046.7(SETX):c.6546+32T>A rs2296873
NM_015046.7(SETX):c.6655-24G>A rs11243704
NM_015046.7(SETX):c.6935+8T>C rs17148873
NM_015046.7(SETX):c.6936-27T>G rs2296866
NM_015046.7(SETX):c.7100+27A>G rs2296865
NM_015046.7(SETX):c.7114G>A (p.Asp2372Asn) rs150673589
NM_015046.7(SETX):c.7759A>G (p.Ile2587Val) rs1056899
NM_015046.7(SETX):c.7834A>G (p.Ser2612Gly) rs3739927

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