ClinVar Genomic variation as it relates to human health
GRCh37/hg19 3q11.2(chr3:96850456-97974150)x3
Germline
Classification
(1)
Uncertain significance
no assertion criteria provided
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 | |||
ARL6 | - | - |
GRCh38 GRCh37 |
248 | 272 | |
CRYBG3 | - | - | - |
GRCh38 GRCh37 |
11 | 36 |
EPHA6 | - | - |
GRCh38 GRCh37 |
67 | 89 | |
GABRR3 | - | - |
GRCh38 GRCh37 |
29 | 52 | |
OR5AC2 | - | - | - |
GRCh38 GRCh37 |
26 | 45 |
OR5H1 | - | - | - |
GRCh38 GRCh37 |
27 | 46 |
OR5H14 | - | - | - |
GRCh38 GRCh37 |
25 | 44 |
OR5H15 | - | - | - |
GRCh38 GRCh37 |
26 | 45 |
RIOX2 | - | - |
GRCh38 GRCh37 |
48 | 68 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jun 21, 2018 | RCV001005454.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022