List of variants in gene BTD reported as benign for not provided

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: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001370658.1(BTD):c.400-285T>C	rs2470529	0.49740
NM_001370658.1(BTD):c.1353T>C (p.Cys451=)	rs3817641	0.08986
NM_001370658.1(BTD):c.399+150T>C	rs9755	0.07318
NM_001370658.1(BTD):c.-16-269G>C	rs6773959	0.04314
NM_001370658.1(BTD):c.249+215A>G	rs73817035	0.03854
NM_001370658.1(BTD):c.-17+290G>A	rs73817023	0.03255
NM_001370658.1(BTD):c.-94C>T	rs114567021	0.01730
NM_001370658.1(BTD):c.1111C>T (p.Pro371Ser)	rs35034250	0.01555
NM_001370658.1(BTD):c.820A>G (p.Ile274Val)	rs35976361	0.01187
NM_001370658.1(BTD):c.1224C>T (p.Tyr408=)	rs35145938	0.01185
NM_001370658.1(BTD):c.73G>A (p.Gly25Arg)	rs34885143	0.01036
NM_001370658.1(BTD):c.585C>T (p.Leu195=)	rs145388314	0.00669
NM_001281723.3(BTD):c.-119G>A	rs2279841
NM_001370658.1(BTD):c.*348del	rs1427846460
NM_001370658.1(BTD):c.*365del	rs1199838348
NM_001370658.1(BTD):c.-17+81A>C	rs115287362
NM_001370658.1(BTD):c.400-271G>C	rs11916854

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.