ClinVar Miner

List of variants in gene SZT2 studied for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP
NM_015284.3(SZT2):c.105C>G (p.Phe35Leu) rs1553138299
NM_015284.3(SZT2):c.2812G>A (p.Ala938Thr) rs143880787
NM_015284.3(SZT2):c.3806C>T (p.Ala1269Val) rs747241860
NM_015284.3(SZT2):c.3964C>T (p.Arg1322Trp) rs752473314
NM_015284.3(SZT2):c.4994G>A (p.Arg1665His) rs562214305
NM_015284.3(SZT2):c.5344C>T (p.Arg1782Cys) rs147748994
NM_015284.3(SZT2):c.5767G>A (p.Val1923Met) rs780805483
NM_015284.3(SZT2):c.6941A>T (p.Glu2314Val) rs1306918506
NM_015284.3(SZT2):c.7716G>A (p.Met2572Ile) rs748723710
NM_015284.3(SZT2):c.8632C>T (p.Arg2878Trp) rs1553154643
NM_015284.3(SZT2):c.8768C>T (p.Thr2923Ile) rs766294629

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.