ClinVar Genomic variation as it relates to human health
GRCh37/hg19 4q34.3-35.1(chr4:181853722-184723116)x1
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 | |||
CDKN2AIP | - | - |
GRCh38 GRCh37 |
34 | 136 | |
CLDN22 | - | - | - |
GRCh38 GRCh37 |
- | 117 |
CLDN24 | - | - | - |
GRCh38 GRCh37 |
11 | 111 |
DCTD | - | - |
GRCh38 GRCh37 |
12 | 120 | |
ING2 | - | - |
GRCh38 GRCh37 |
6 | 104 | |
RWDD4 | - | - | - |
GRCh38 GRCh37 |
9 | 114 |
TENM3 | - | - |
GRCh38 GRCh37 |
406 | 515 | |
TRAPPC11 | - | - |
GRCh38 GRCh37 |
869 | 1056 | |
WWC2 | - | - | - |
GRCh38 GRCh37 |
63 | 188 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Oct 9, 2019 | RCV001259889.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022