ClinVar Genomic variation as it relates to human health
GRCh38/hg38 19p13.3(chr19:3437996-4039217)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 | |||
APBA3 | - | - |
GRCh38 GRCh37 |
69 | 93 | |
ATCAY | - | - |
GRCh38 GRCh37 |
192 | 220 | |
CACTIN | - | - |
GRCh38 GRCh37 |
17 | 52 | |
CACTIN-AS1 | - | - | - | GRCh38 | - | 22 |
DAPK3 | - | - |
GRCh38 GRCh37 |
21 | 48 | |
DOHH | - | - |
GRCh38 GRCh37 |
33 | 58 | |
EEF2 | - | - |
GRCh38 GRCh37 |
369 | 424 | |
FZR1 | - | - |
GRCh38 GRCh37 |
29 | 54 | |
GIPC3 | - | - |
GRCh38 GRCh37 |
189 | 215 | |
HMG20B | - | - |
GRCh38 GRCh37 |
12 | 37 |
There are 63 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Dec 22, 2010 | RCV000135779.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024