ClinVar Genomic variation as it relates to human health
GRCh37/hg19 14q11.2(chr14:21589998-21999445)x1
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 | |||
CHD8 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1235 | 1335 | |
OR5AU1 | - | No evidence available | No evidence available |
GRCh38 GRCh37 |
19 | 58 |
SUPT16H | No evidence available | No evidence available |
GRCh38 GRCh37 |
74 | 134 | |
HNRNPC | - | - |
GRCh38 GRCh37 |
13 | 63 | |
METTL3 | - | - |
GRCh38 GRCh37 |
13 | 51 | |
RAB2B | - | - |
GRCh38 GRCh37 |
7 | 48 | |
RPGRIP1 | - | - |
GRCh38 GRCh37 |
1018 | 1071 | |
SALL2 | - | - |
GRCh38 GRCh37 |
108 | 144 | |
TOX4 | - | - |
GRCh38 GRCh37 |
32 | 74 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Aug 31, 2018 | RCV001006608.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022