ClinVar Genomic variation as it relates to human health
chr1:17555508-24706269 complex variant
Germline
Classification
(1)
Uncertain significance
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 | |||
ACTL8 | - | - | - |
GRCh38 GRCh37 |
20 | 44 |
AKR7A2 | - | - |
GRCh38 GRCh37 |
24 | 46 | |
AKR7A3 | - | - |
GRCh38 GRCh37 |
37 | 59 | |
AKR7L | - | - |
GRCh38 GRCh37 |
- | 22 | |
ALDH4A1 | - | - |
GRCh38 GRCh37 |
273 | 330 | |
ALPL | - | - |
GRCh38 GRCh37 |
1180 | 1195 | |
ARHGEF10L | - | - |
GRCh38 GRCh37 |
81 | 102 | |
ASAP3 | - | - |
GRCh38 GRCh38 GRCh37 |
52 | 61 | |
C1QA | - | - |
GRCh38 GRCh37 |
132 | 144 | |
C1QB | - | - |
GRCh38 GRCh37 |
101 | 112 |
There are 80 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) |
|
Jul 20, 2015 | RCV000207266.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 14, 2024