ClinVar Genomic variation as it relates to human health
GRCh38/hg38 4q35.1(chr4:183235127-183370360)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 | |||
CLDN22 | - | - | - |
GRCh38 GRCh37 |
- | 117 |
CLDN24 | - | - | - |
GRCh38 GRCh37 |
11 | 111 |
LOC126807235 | - | - | - | GRCh38 | - | 45 |
LOC126807236 | - | - | - | GRCh38 | - | 45 |
LOC129993431 | - | - | - | GRCh38 | - | 46 |
LOC132089104 | - | - | - | GRCh38 | - | 45 |
WWC2 | - | - |
GRCh38 GRCh37 |
63 | 188 | |
WWC2-AS1 | - | - | GRCh38 | - | 47 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 30, 2010 | RCV000141310.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023