ClinVar Genomic variation as it relates to human health
GRCh37/hg19 19p13.13-13.11(chr19:13970692-18139376)x3
Germline
Classification
(1)
Uncertain significance
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 | |||
ABHD8 | - | - | - |
GRCh38 GRCh37 |
- | 36 |
ADGRE2 | - | - |
GRCh38 GRCh37 |
459 | 477 | |
ADGRE3 | - | - |
GRCh38 GRCh37 |
37 | 56 | |
ADGRE5 | - | - |
GRCh38 GRCh37 |
49 | 91 | |
ADGRL1 | - | - |
GRCh38 GRCh38 GRCh37 |
7 | 148 | |
AKAP8 | - | - |
GRCh38 GRCh37 |
93 | 113 | |
AKAP8L | - | - |
GRCh38 GRCh37 |
34 | 62 | |
ANKLE1 | - | - |
GRCh38 GRCh37 |
75 | 93 | |
ANO8 | - | - |
GRCh38 GRCh37 |
78 | 105 | |
AP1M1 | - | - |
GRCh38 GRCh37 |
13 | 30 |
There are 101 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
- | RCV003986122.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 30, 2024