List of variants in gene combination SCN1A, SCN9A reported as likely benign by Athena Diagnostics Inc

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: 7

Download table as spreadsheet

HGVS	dbSNP
NM_001365536.1(SCN9A):c.2248A>G (p.Ile750Val)	rs182650126
NM_001365536.1(SCN9A):c.2766C>T (p.Arg922=)	rs199653503
NM_001365536.1(SCN9A):c.2964C>T (p.Leu988=)	rs201430964
NM_001365536.1(SCN9A):c.3361C>T (p.Arg1121Trp)	rs190664764
NM_001365536.1(SCN9A):c.4645T>C (p.Trp1549Arg)	rs202084411
NM_001365536.1(SCN9A):c.4953C>G (p.Leu1651=)	rs776545037
NM_001365536.1(SCN9A):c.5779C>T (p.Leu1927Phe)	rs111558968

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.