List of variants in gene ROM1 reported as benign for perceptual disorders

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_000327.4(ROM1):c.669G>C (p.Arg223=)	rs1801144	0.26271
NM_000327.3(ROM1):c.-329G>T	rs3923805	0.21125
NM_000327.3(ROM1):c.-438G>A	rs576371643	0.00715
NM_000327.4(ROM1):c.812T>C (p.Met271Thr)	rs137950927	0.00178
NM_000327.4(ROM1):c.47G>A (p.Arg16His)	rs143166696	0.00125
NM_000327.4(ROM1):c.342C>T (p.Leu114=)	rs537377404	0.00049
NM_000327.4(ROM1):c.339dup (p.Leu114fs)	rs71458427	0.00033
NM_000327.4(ROM1):c.512G>A (p.Arg171His)	rs150926409	0.00026
NM_000327.4(ROM1):c.724C>T (p.Arg242Ter)	rs147065010	0.00011
NM_000327.4(ROM1):c.422T>C (p.Leu141Ser)	rs190642059	0.00002
NM_000327.4(ROM1):c.967T>C (p.Trp323Arg)

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.