ClinVar Genomic variation as it relates to human health
GRCh38/hg38 12q23.2(chr12:102123861-102457250)x1
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 | |||
IGF1 | - | - |
GRCh38 GRCh37 |
5 | 203 | |
LINC02456 | - | - | - | GRCh38 | - | 192 |
LOC126861613 | - | - | - | GRCh38 | - | 3 |
LOC129390543 | - | - | - | GRCh38 | - | 3 |
LOC129390544 | - | - | - | GRCh38 | - | 3 |
LOC130008567 | - | - | - | GRCh38 | - | 3 |
LOC132089961 | - | - | - | GRCh38 | - | 3 |
LOC132089962 | - | - | - | GRCh38 | - | 3 |
LOC132089963 | - | - | - | GRCh38 | - | 3 |
LOC132089964 | - | - | - | GRCh38 | - | 3 |
There are 2 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Likely benign (1) |
|
Apr 4, 2013 | RCV000139920.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024