ClinVar Genomic variation as it relates to human health
GRCh37/hg19 2q37.3(chr2:240541136-242783384)x1
Germline
Classification
(1)
Likely pathogenic
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 | |||
KIF1A | No evidence available | No evidence available |
GRCh38 GRCh37 |
2849 | 3052 | |
AGXT | - | - |
GRCh38 GRCh37 |
895 | 1010 | |
ANKMY1 | - | - | - |
GRCh38 GRCh37 |
83 | 204 |
ANO7 | - | - |
GRCh38 GRCh37 |
180 | 333 | |
AQP12A | - | - |
GRCh38 GRCh37 |
20 | 127 | |
AQP12B | - | - | - |
GRCh38 GRCh37 |
42 | 147 |
ATG4B | - | - |
GRCh38 GRCh37 |
34 | 153 | |
BOK | - | - |
GRCh38 GRCh37 |
12 | 133 | |
CAPN10 | - | - |
GRCh38 GRCh37 |
91 | 199 | |
COPS9 | - | - |
GRCh38 GRCh37 |
1 | 99 |
There are 25 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely pathogenic (1) |
|
Jul 7, 2014 | RCV000510186.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024