ClinVar Miner

List of variants in gene combination LOC102724058, SCN1A reported as uncertain significance for Familial hemiplegic migraine

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
Download table as spreadsheet
HGVS dbSNP
NM_001165963.1(SCN1A):c.*1121T>C rs886055034
NM_001165963.1(SCN1A):c.*129T>G rs886055040
NM_001165963.1(SCN1A):c.*1482G>A rs886055033
NM_001165963.1(SCN1A):c.*1795G>A rs189183531
NM_001165963.1(SCN1A):c.*1872delT rs878898132
NM_001165963.1(SCN1A):c.*1950G>A rs773354801
NM_001165963.1(SCN1A):c.*1989C>T rs371391758
NM_001165963.1(SCN1A):c.*259T>C rs886055039
NM_001165963.1(SCN1A):c.*460A>C rs746164130
NM_001165963.1(SCN1A):c.*672_*675delGCTT rs886055038
NM_001165963.1(SCN1A):c.*878dupT rs886055037
NM_001165963.1(SCN1A):c.*912T>A rs886055036
NM_001165963.1(SCN1A):c.*977T>C rs886055035
NM_001165963.1(SCN1A):c.3513T>C (p.Pro1171=) rs886055044
NM_001165963.1(SCN1A):c.3573T>C (p.Cys1191=) rs750943685
NM_001165963.1(SCN1A):c.3880-10G>C rs886055043
NM_001165963.1(SCN1A):c.4581+12C>T rs886055042
NM_001165963.1(SCN1A):c.4731T>C (p.Asn1577=) rs145296488
NM_001165963.1(SCN1A):c.4941A>G (p.Leu1647=) rs770111331
NM_001165963.1(SCN1A):c.5992G>C (p.Glu1998Gln) rs886055041

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.