ClinVar Genomic variation as it relates to human health
NM_206933.4(USH2A):c.5012G>A (p.Gly1671Asp)
Germline
Top reviewed classifications are shown here.
Submission summary:
Reviewed by expert panel
Pathogenic
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
USH2A | - | - |
GRCh38 GRCh37 |
6944 | 8419 | |
USH2A-AS2 | - | - | - | GRCh38 | - | 550 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Aug 8, 2014 | RCV000156571.13 | |
Likely pathogenic (1) |
|
Jan 1, 2015 | RCV000505112.8 | |
Conflicting interpretations of pathogenicity (3) |
|
Jan 31, 2024 | RCV000725477.23 | |
Likely pathogenic (2) |
|
Dec 31, 2022 | RCV001004787.11 | |
Likely pathogenic (1) |
|
Oct 25, 2023 | RCV003462063.1 | |
Pathogenic (1) |
|
Feb 27, 2024 | RCV003991016.1 | |
Likely pathogenic (1) |
|
Oct 11, 2022 | RCV004528894.1 |
Citations for germline classification of this variant
HelpText-mined citations for rs727505116 ...
HelpThese citations are identified by LitVar using
the rs number, so they may include citations for more than one variant
at this location. Please review the LitVar results carefully for your
variant of interest.
Record last updated Jun 10, 2024