ClinVar Miner

List of variants reported as likely pathogenic for neurodevelopmental disorder by Johns Hopkins Genomics, Johns Hopkins University

Included ClinVar conditions (779):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001032221.6(STXBP1):c.703C>G (p.Arg235Gly) rs796053359
NM_001127222.2(CACNA1A):c.3989+1G>C rs587776693
NM_001271.4(CHD2):c.2809C>G (p.His937Asp) rs1596429174
NM_014712.3(SETD1A):c.3005_3006del (p.Glu1002fs)
NM_031263.4(HNRNPK):c.620_637del (p.Lys207_Leu212del)
NM_177559.3(CSNK2A1):c.367-1G>A rs2018375840
NM_182641.4(BPTF):c.8625dup (p.Asn2876Ter) rs1599044870

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.