List of variants in gene combination IFT172, KRTCAP3 reported as benign for retinal disorder

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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_015662.3(IFT172):c.*2T>C	rs4803	0.47361
NM_015662.3(IFT172):c.4745T>C (p.Ile1582Thr)	rs61742074	0.00712
NM_015662.3(IFT172):c.4755+9G>C	rs375261962	0.00135
NM_015662.3(IFT172):c.5161-20G>A	rs372154058	0.00076
NM_015662.3(IFT172):c.4933G>A (p.Val1645Ile)	rs149117098	0.00046
NM_015662.3(IFT172):c.4815+9G>A	rs199667794	0.00019
NM_015662.3(IFT172):c.5187C>T (p.Asp1729=)	rs143671920	0.00015
NM_015662.3(IFT172):c.4990C>T (p.Arg1664Trp)	rs139348179	0.00005

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.