ClinVar Miner

List of variants in gene SLC6A2 reported by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001172501.3(SLC6A2):c.*416del rs113163898 0.03045
NM_001172501.3(SLC6A2):c.*414_*415insC rs886052137 0.00029
NM_001172501.3(SLC6A2):c.*306C>T rs192171814 0.00001
NM_001172501.3(SLC6A2):c.*1017G>A rs886052141
NM_001172501.3(SLC6A2):c.*396_*397dup rs35571499
NM_001172501.3(SLC6A2):c.*401_*402insCA rs201774381
NM_001172501.3(SLC6A2):c.*414_*415dup rs72297759
NM_001172501.3(SLC6A2):c.*415dup rs72297759
NM_001172501.3(SLC6A2):c.*919_*921del rs540636734

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.