List of variants in gene RP2 reported as benign for Retinitis pigmentosa

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_006915.3(RP2):c.*828G>A	rs4239962	0.99135
NM_006915.3(RP2):c.844C>T (p.Arg282Trp)	rs1805147	0.01917
NM_006915.3(RP2):c.*2085T>C	rs73478384	0.00737
NM_006915.3(RP2):c.*2163T>C	rs35931067	0.00576
NM_006915.3(RP2):c.*958A>C	rs190692640	0.00507
NM_006915.3(RP2):c.*435C>T	rs147975002	0.00468
NM_006915.3(RP2):c.606T>C (p.Pro202=)	rs144795993	0.00377
NM_006915.3(RP2):c.601A>G (p.Ile201Val)	rs149503319	0.00307
NM_006915.3(RP2):c.*904A>G	rs144870840	0.00074
NM_006915.3(RP2):c.*2156A>G	rs141748740	0.00066
NM_006915.3(RP2):c.*1908G>A	rs782216739

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.