ClinVar Miner

List of variants studied for schizophrenia by Juno Genomics, Hangzhou Juno Genomics, Inc

Included ClinVar conditions (15):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005957.5(MTHFR):c.1316T>C (p.Leu439Pro) rs545086633 0.00001
NM_001330078.2(NRXN1):c.1753C>T (p.Arg585Trp)
NM_001330078.2(NRXN1):c.3499C>T (p.Arg1167Ter) rs199546979
NM_001330078.2(NRXN1):c.656_664dup (p.Ala219_Glu221dup) rs546508545
NM_001372044.2(SHANK3):c.1529+3_1529+4insGAGG
NM_001372044.2(SHANK3):c.3865dup (p.Ala1289fs) rs2146831793
NM_005957.5(MTHFR):c.1429C>T (p.Gln477Ter)
NM_005957.5(MTHFR):c.976G>A (p.Glu326Lys)

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.