ClinVar Genomic variation as it relates to human health
GRCh38/hg38 3q13.31-13.32(chr3:114734452-118164045)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 | |||
GAP43 | - | - |
GRCh38 GRCh37 |
15 | 49 | |
LINC00901 | - | - | - | GRCh38 | - | 11 |
LINC00903 | - | - | - | GRCh38 | - | 12 |
LINC02024 | - | - | - | GRCh38 | - | 11 |
LINC03051 | - | - | - | GRCh38 | - | 12 |
LOC101926953 | - | - | - | GRCh38 | - | 11 |
LOC108004532 | - | - | - | GRCh38 | - | 14 |
LOC110121175 | - | - | - | GRCh38 | - | 20 |
LOC126806776 | - | - | - | GRCh38 | - | 20 |
LOC126806777 | - | - | - | GRCh38 | - | 20 |
There are 29 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
|
Uncertain significance (1) |
|
Nov 5, 2013 | RCV000143674.7 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024