ClinVar Miner

List of variants in gene LPAR6, RB1 studied for Hypotrichosis 8

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001162498.3(LPAR6):c.565G>A (p.Glu189Lys) rs121434309 0.00001
NM_001162498.3(LPAR6):c.107G>A (p.Cys36Tyr) rs2138203806
NM_001162498.3(LPAR6):c.145C>T (p.Arg49Ter)
NM_001162498.3(LPAR6):c.188A>T (p.Asp63Val) rs879255262
NM_001162498.3(LPAR6):c.1A>G (p.Met1Val) rs2138204557
NM_001162498.3(LPAR6):c.207_210dup (p.Pro71fs)
NM_001162498.3(LPAR6):c.373_374del (p.Lys125fs) rs1566212378
NM_001162498.3(LPAR6):c.436G>A (p.Gly146Arg) rs121434308
NM_001162498.3(LPAR6):c.463C>T (p.Gln155Ter) rs121434306
NM_001162498.3(LPAR6):c.562A>T (p.Ile188Phe) rs121434307
NM_001162498.3(LPAR6):c.587C>T (p.Pro196Leu) rs115596308
NM_001162498.3(LPAR6):c.66_69dup (p.Phe24fs) rs558917628
NM_001162498.3(LPAR6):c.742A>T (p.Asn248Tyr)
NM_001162498.3(LPAR6):c.830T>C (p.Leu277Pro)
NM_001162498.3(LPAR6):c.833G>A (p.Cys278Tyr)
NM_001162498.3(LPAR6):c.8G>C (p.Ser3Thr)

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.