ClinVar Miner

List of variants in gene ARL6 studied for Retinitis pigmentosa

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001278293.3(ARL6):c.480-8C>T rs77010939 0.01364
NM_001278293.3(ARL6):c.*255C>T rs79196822 0.01359
NM_001278293.3(ARL6):c.*495C>T rs188498639 0.00186
NM_001278293.3(ARL6):c.-137A>C rs192372191 0.00174
NM_001278293.3(ARL6):c.*470G>A rs184213166 0.00067
NM_177976.3(ARL6):c.-375C>T rs536935620 0.00052
NM_001278293.3(ARL6):c.-207G>A rs189005414 0.00027
NM_001278293.3(ARL6):c.-71C>G rs777066573 0.00027
NM_001278293.3(ARL6):c.365G>A (p.Arg122Gln) rs142258123 0.00006
NM_001278293.3(ARL6):c.121A>G (p.Asn41Asp) rs201618364 0.00005
NM_001278293.3(ARL6):c.536-4T>C rs201939836 0.00004
NM_001278293.3(ARL6):c.266C>G (p.Ala89Gly) rs587777805 0.00002
NM_001278293.3(ARL6):c.281T>C (p.Ile94Thr) rs771054395 0.00002
NM_001278293.3(ARL6):c.*309T>C rs2038100273 0.00001
NM_001278293.3(ARL6):c.-146T>C rs886058937 0.00001
NM_001278293.3(ARL6):c.306G>A (p.Met102Ile) rs763779778 0.00001
NM_001278293.3(ARL6):c.*275G>A rs886058939
NM_001278293.3(ARL6):c.-27-1461A>T rs143739859
NM_001278293.3(ARL6):c.266C>A (p.Ala89Asp) rs587777805
NM_001278293.3(ARL6):c.341A>G (p.Asn114Ser) rs2037385151
NM_001278293.3(ARL6):c.365G>C (p.Arg122Pro) rs142258123
NM_001278293.3(ARL6):c.526T>C (p.Trp176Arg) rs886058938
NM_001278293.3(ARL6):c.92C>T (p.Thr31Met) rs104893680
NM_177976.3(ARL6):c.-371A>G rs754624462

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.