List of variants reported as likely benign for TRPV4-related bone disorder by Illumina Laboratory Services, Illumina

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
NR_039718.1(MIR4497):n.66C>T	rs56079803	0.02373
NM_021625.5(TRPV4):c.1584C>T (p.Asn528=)	rs142749412	0.00016
NM_021625.5(TRPV4):c.2320C>T (p.Arg774Cys)	rs145102919	0.00007
NM_021625.5(TRPV4):c.2484C>T (p.Arg828=)	rs142656819	0.00006
NM_021625.5(TRPV4):c.2605G>A (p.Ala869Thr)	rs138396764	0.00006
NM_021625.5(TRPV4):c.958C>T (p.Arg320Ter)	rs142902080	0.00006
NM_021625.5(TRPV4):c.963C>A (p.Gly321=)	rs148534854	0.00006
NM_021625.5(TRPV4):c.205A>C (p.Met69Leu)	rs200199102	0.00004
NM_021625.5(TRPV4):c.1211G>A (p.Arg404His)	rs377257364	0.00003
NM_021625.5(TRPV4):c.523A>G (p.Thr175Ala)	rs146304351	0.00002
NM_021625.5(TRPV4):c.1390C>T (p.Arg464Cys)	rs373049874	0.00001
NM_021625.5(TRPV4):c.1700A>T (p.Tyr567Phe)	rs763889344	0.00001
NM_021625.5(TRPV4):c.2439C>T (p.Thr813=)	rs545589086	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.