List of variants in gene SCN2A reported as benign by Genetic Services Laboratory, University of Chicago

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: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001040142.2(SCN2A):c.1035-3T>C	rs2121371	0.82016
NM_001040142.2(SCN2A):c.4914T>A (p.Arg1638=)	rs2060198	0.25169
NM_001040142.2(SCN2A):c.1785T>C (p.Asp595=)	rs141815642	0.01027
NM_001040142.2(SCN2A):c.1842G>T (p.Pro614=)	rs114315466	0.00790
NM_001040142.2(SCN2A):c.2723A>G (p.Lys908Arg)	rs2228980	0.00365
NM_001040142.2(SCN2A):c.5910G>A (p.Thr1970=)	rs75057869	0.00190
NM_001040142.2(SCN2A):c.3453C>T (p.Pro1151=)	rs145662546	0.00166
NM_001040142.2(SCN2A):c.5757C>T (p.Tyr1919=)	rs140417984	0.00069
NM_001040142.2(SCN2A):c.960T>C (p.Ile320=)	rs185590667	0.00014
NM_001040142.2(SCN2A):c.4989C>T (p.Ile1663=)	rs373347369	0.00010
NM_001040142.2(SCN2A):c.1725G>A (p.Ala575=)	rs543538780	0.00008
NM_001040142.2(SCN2A):c.3372C>T (p.Ser1124=)	rs571408286	0.00008
NM_001040142.2(SCN2A):c.1959G>A (p.Val653=)	rs200546427	0.00006
NM_001040142.2(SCN2A):c.3457G>A (p.Glu1153Lys)	rs200138205

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.