ClinVar Genomic variation as it relates to human health
GRCh38/hg38 2q24.1-31.1(chr2:154294042-175989372)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 | |||
NR4A2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
119 | 155 | |
SCN1A | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
2181 | 4528 | |
SCN2A | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
2523 | 2598 | |
TBR1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
204 | 244 | |
SLC4A10 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
87 | 113 | |
DLX1 | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh37 |
8 | 31 | |
DLX2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
19 | 41 | |
SLC25A12 | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh37 |
486 | 512 | |
ABCB11 | - | - |
GRCh38 GRCh38 GRCh37 |
1451 | 1551 | |
ACVR1 | - | - |
GRCh38 GRCh37 |
308 | 328 |
There are 522 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 |
---|---|---|---|---|
Pathogenic (1) |
|
Mar 10, 2014 | RCV000142286.7 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024