List of variants in gene combination LOC126807546, SH3TC2 reported as uncertain significance for Susceptibility to mononeuropathy of the median nerve, mild

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_024577.4(SH3TC2):c.*20469C>T	rs886060097	0.00026
NM_024577.4(SH3TC2):c.*20400A>C	rs1019391321	0.00011
NM_024577.4(SH3TC2):c.*19631T>A	rs961541157	0.00010
NM_024577.4(SH3TC2):c.*20362T>C	rs571268825	0.00010
NM_024577.4(SH3TC2):c.*20412A>T	rs774453230	0.00009
NM_024577.4(SH3TC2):c.*20618C>T	rs370869298	0.00002
NM_024577.4(SH3TC2):c.*20230G>T	rs761890589	0.00001
NM_024577.4(SH3TC2):c.*20553A>G	rs1419202542	0.00001
NM_024577.4(SH3TC2):c.*19552G>T	rs1410058775
NM_024577.4(SH3TC2):c.*20086A>G	rs1753304105
NM_024577.4(SH3TC2):c.*20135C>T	rs1753303246

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.