List of variants in gene combination LPAR6, RB1 reported as benign

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001162498.3(LPAR6):c.-473T>C	rs2227311	0.10940
NM_001162498.3(LPAR6):c.*86C>A	rs4151551	0.05974
NM_001162498.3(LPAR6):c.921G>T (p.Trp307Cys)	rs17071686	0.00841
NM_000321.3(RB1):c.1695+30396A>G	rs2233573
NM_000321.3(RB1):c.1696-30191del	rs66618985
NM_001162498.3(LPAR6):c.341_344del (p.Arg114fs)	rs1198561901
NM_001162498.3(LPAR6):c.347del (p.Leu116fs)	rs1404056158
NM_001162498.3(LPAR6):c.350_352del (p.Ala117_Ile118delinsVal)	rs1200570253
NM_001162498.3(LPAR6):c.354T>G (p.Ile118Met)	rs1458608158
NM_001162498.3(LPAR6):c.358T>G (p.Tyr120Asp)	rs1344531248
NM_001162498.3(LPAR6):c.359del (p.Tyr120fs)	rs1275629547
NM_001162498.3(LPAR6):c.361_362insGTAT (p.Pro121fs)	rs1236830240
NM_001162498.3(LPAR6):c.366T>A (p.Phe122Leu)	rs977436301

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.