List of variants in gene SETX reported as likely benign for not specified

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

Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_015046.7(SETX):c.3576T>G (p.Asp1192Glu)	rs1185193	0.76694
NM_015046.7(SETX):c.1077T>C (p.Tyr359=)	rs9411449	0.75774
NM_015046.7(SETX):c.3754G>A (p.Gly1252Arg)	rs1183768	0.68476
NM_015046.7(SETX):c.4156A>G (p.Ile1386Val)	rs543573	0.68049
NM_015046.7(SETX):c.7759A>G (p.Ile2587Val)	rs1056899	0.44536
NM_015046.7(SETX):c.5563A>G (p.Thr1855Ala)	rs2296871	0.31596
NM_015046.7(SETX):c.5811T>C (p.Asp1937=)	rs2296869	0.31585
NM_015046.7(SETX):c.3455T>G (p.Phe1152Cys)	rs3739922	0.04708
NM_015046.7(SETX):c.7640T>C (p.Ile2547Thr)	rs151117904	0.00431
NM_015046.7(SETX):c.472T>G (p.Leu158Val)	rs145438764	0.00347
NM_015046.7(SETX):c.4660T>G (p.Cys1554Gly)	rs112089123	0.00250
NM_015046.7(SETX):c.4982C>G (p.Pro1661Arg)	rs146873848	0.00080
NM_015046.7(SETX):c.5949+5G>A	rs374656811	0.00078
NM_015046.7(SETX):c.7870G>T (p.Asp2624Tyr)	rs141589525	0.00073
NM_015046.7(SETX):c.2479A>G (p.Lys827Glu)	rs150532677	0.00058
NM_015046.7(SETX):c.4197A>G (p.Thr1399=)	rs148078248	0.00052
NM_015046.7(SETX):c.3345C>G (p.Ala1115=)	rs142020270	0.00039
NM_015046.7(SETX):c.968G>A (p.Ser323Asn)	rs372193033	0.00019
NM_015046.7(SETX):c.6013G>A (p.Val2005Met)	rs148568105	0.00016
NM_015046.7(SETX):c.390C>T (p.Asn130=)	rs138363625	0.00014
NM_015046.7(SETX):c.3090T>C (p.Leu1030=)	rs368677513	0.00011
NM_015046.7(SETX):c.4866G>A (p.Pro1622=)	rs779472573	0.00009
NM_015046.7(SETX):c.1221A>G (p.Thr407=)	rs377618570	0.00008
NM_015046.7(SETX):c.1626C>T (p.Leu542=)	rs746541015	0.00004
NM_015046.7(SETX):c.3029G>A (p.Arg1010His)	rs370781594	0.00004
NM_015046.7(SETX):c.3810G>A (p.Pro1270=)	rs753022992	0.00004
NM_015046.7(SETX):c.6122T>C (p.Ile2041Thr)	rs140676924	0.00004
NM_015046.7(SETX):c.719-40T>G	rs756527948	0.00004
NM_015046.7(SETX):c.5781+9T>C	rs772671321	0.00003
NM_015046.7(SETX):c.5825T>C (p.Ile1942Thr)	rs773379832	0.00001
NM_015046.7(SETX):c.5950-14G>A	rs375632375	0.00001
NM_015046.7(SETX):c.7749C>T (p.Asp2583=)	rs754701648

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