List of variants in gene PRPH2 reported as likely 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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000322.5(PRPH2):c.1013A>G (p.Asp338Gly)	rs434102	0.77412
NM_000322.5(PRPH2):c.133C>T (p.Leu45Phe)	rs61755770	0.00414
NM_000322.5(PRPH2):c.866C>T (p.Ser289Leu)	rs62645939	0.00079
NM_000322.5(PRPH2):c.249C>T (p.Tyr83=)	rs61755775	0.00053
NM_000322.5(PRPH2):c.938C>T (p.Pro313Leu)	rs61748434	0.00044
NM_000322.5(PRPH2):c.252C>T (p.Asp84=)	rs139936445	0.00017
NM_000322.5(PRPH2):c.801C>T (p.Val267=)	rs189358082	0.00002
NM_000322.5(PRPH2):c.*484dup	rs55851577
NM_000322.5(PRPH2):c.387C>T (p.Thr129=)	rs1582780697
NM_000322.5(PRPH2):c.483C>G (p.Ile161Met)	rs76989855

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.