List of variants in gene USH2A reported as not provided by NEI Ophthalmic Genomics Laboratory, National Institutes of Health

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_206933.4(USH2A):c.2137G>C (p.Gly713Arg)	rs696723	0.06184
NM_206933.4(USH2A):c.1931A>T (p.Asp644Val)	rs1805048	0.04940
NM_206933.4(USH2A):c.9343A>G (p.Thr3115Ala)	rs56032526	0.03269
NM_206933.4(USH2A):c.6875G>A (p.Arg2292His)	rs41277210	0.02015
NM_206933.4(USH2A):c.6713A>C (p.Glu2238Ala)	rs41277212	0.01991
NM_206933.4(USH2A):c.13297G>T (p.Val4433Leu)	rs111033381	0.01895
NM_206933.4(USH2A):c.15091C>T (p.Arg5031Trp)	rs56038610	0.01377
NM_206933.4(USH2A):c.7584C>T (p.Thr2528=)	rs78250390	0.00976
NM_206933.4(USH2A):c.4714C>T (p.Leu1572Phe)	rs111033333	0.00063
NM_206933.4(USH2A):c.14792-2A>G	rs137853923	0.00002

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.