ClinVar Genomic variation as it relates to human health
GRCh38/hg38 2q36.3-37.2(chr2:228014149-234976424)x3
Germline
Classification
(1)
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 | |||
TRIP12 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
401 | 455 | |
DIS3L2 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
2281 | 2326 | |
GIGYF2 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
140 | 404 | |
SPP2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
183 | 230 | |
ALPG | - | - |
GRCh38 GRCh37 |
31 | 106 | |
ALPI | - | - |
GRCh38 GRCh37 |
66 | 107 | |
ALPP | - | - |
GRCh38 GRCh37 |
73 | 113 | |
ARL4C | - | - |
GRCh38 GRCh37 |
9 | 55 | |
ARMC9 | - | - |
GRCh38 GRCh37 |
615 | 681 | |
ATG16L1 | - | - |
GRCh38 GRCh38 GRCh37 |
32 | 74 |
There are 301 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Pathogenic (1) |
|
Sep 16, 2011 | RCV000136967.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 01, 2024