ClinVar Genomic variation as it relates to human health
GRCh37/hg19 2q24.2-31.1(chr2:160347642-174075851)x1
Germline
Classification
(1)
Pathogenic
criteria provided, single submitter
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 | |||
SCN1A | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
2208 | 4573 | |
SCN2A | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
2554 | 2629 | |
TBR1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
216 | 256 | |
SLC4A10 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
95 | 121 | |
DLX1 | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh37 |
11 | 34 | |
DLX2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
20 | 42 | |
SLC25A12 | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh37 |
488 | 514 | |
ABCB11 | - | - |
GRCh38 GRCh38 GRCh37 |
1484 | 1586 | |
B3GALT1 | - | - |
GRCh38 GRCh37 |
1 | 42 | |
BAZ2B | - | - |
GRCh38 GRCh37 |
184 | 244 |
There are 59 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) |
|
Feb 2, 2022 | RCV002271993.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jun 23, 2024