ClinVar Genomic variation as it relates to human health
GRCh37/hg19 2q31.1(chr2:171667051-176832848)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 | |||
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 | |
ATF2 | - | - |
GRCh38 GRCh37 |
21 | 55 | |
ATP5MC3 | - | - |
GRCh38 GRCh37 |
18 | 52 | |
CDCA7 | - | - |
GRCh38 GRCh37 |
224 | 248 | |
CHN1 | - | - |
GRCh38 GRCh37 |
94 | 136 | |
CHRNA1 | - | - |
GRCh38 GRCh37 |
488 | 523 | |
CIR1 | - | - |
GRCh38 GRCh37 |
23 | 59 | |
CYBRD1 | - | - |
GRCh38 GRCh37 |
17 | 44 |
There are 19 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 |
---|---|---|---|---|
Pathogenic (1) |
|
Jul 20, 2017 | RCV000682159.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023