List of variants reported as likely benign for Retinitis pigmentosa 28

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001201543.2(FAM161A):c.1665G>A (p.Leu555=)	rs6545910	0.10308
NM_001201543.2(FAM161A):c.1133T>G (p.Leu378Arg)	rs187695569	0.00389
NM_001201543.2(FAM161A):c.197C>T (p.Thr66Ile)	rs145199539	0.00372
NM_001201543.2(FAM161A):c.1153C>G (p.Gln385Glu)	rs139266382	0.00309
NM_001201543.2(FAM161A):c.1551G>A (p.Thr517=)	rs143622468	0.00248
NM_001201543.2(FAM161A):c.2064T>C (p.Ile688=)	rs138464813	0.00145
NM_001201543.2(FAM161A):c.1989C>T (p.Val663=)	rs201362403	0.00131
NM_001201543.2(FAM161A):c.720G>A (p.Glu240=)	rs750749446	0.00007
NM_001201543.2(FAM161A):c.228G>A (p.Pro76=)	rs776173729	0.00004
NM_001201543.2(FAM161A):c.1473G>A (p.Leu491=)	rs551187535	0.00001
NM_001201543.2(FAM161A):c.171C>T (p.Pro57=)	rs764002326	0.00001
NM_001201543.2(FAM161A):c.246T>C (p.Phe82=)	rs777320853	0.00001
NM_001201543.2(FAM161A):c.678G>A (p.Arg226=)	rs1442927125	0.00001

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.