ClinVar Genomic variation as it relates to human health
GRCh38/hg38 2p24.1(chr2:19667198-20009783)x3
Germline
Classification
(1)
Likely benign
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 | |||
MATN3 | No evidence available | No evidence available |
GRCh38 GRCh37 |
158 | 307 | |
LINC00954 | - | - | - | GRCh38 | - | 11 |
LOC105373461 | - | - | - | GRCh38 | - | 11 |
LOC126806163 | - | - | - | GRCh38 | - | 11 |
LOC129933185 | - | - | - | GRCh38 | - | 11 |
LOC129933186 | - | - | - | GRCh38 | - | 19 |
LOC129933187 | - | - | - | GRCh38 | - | 11 |
TTC32 | - | - | - |
GRCh38 GRCh37 |
12 | 36 |
WDR35 | - | - |
GRCh38 GRCh37 |
644 | 682 | |
WDR35-DT | - | - | - | GRCh38 | - | 137 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Likely benign (1) |
|
Jul 18, 2014 | RCV000142182.7 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024