ClinVar Genomic variation as it relates to human health
GRCh38/hg38 2p25.3(chr2:848908-1110952)x3
Germline
Classification
(1)
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 | |||
LINC01115 | - | - | - |
GRCh38 GRCh38 |
- | 32 |
LINC01939 | - | - | - | GRCh38 | - | 33 |
LOC126806099 | - | - | - |
GRCh38 GRCh38 |
- | 30 |
LOC126806100 | - | - | - | GRCh38 | - | 31 |
LOC126806101 | - | - | - | GRCh38 | - | 30 |
LOC129932979 | - | - | - | GRCh38 | - | 31 |
LOC129932980 | - | - | - | GRCh38 | - | 32 |
SNTG2 | - | - |
GRCh38 GRCh38 GRCh38 GRCh37 |
77 | 155 | |
SNTG2-AS1 | - | - | - | GRCh38 | - | 35 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Benign (1) |
|
Apr 30, 2011 | RCV000141065.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023