ClinVar Genomic variation as it relates to human health
GRCh37/hg19 1q21.3-22(chr1:154898854-155242457)x3
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 | |||
ADAM15 | - | - |
GRCh38 GRCh37 |
- | 97 | |
CKS1B | - | - |
GRCh38 GRCh37 |
2 | 20 | |
CLK2 | - | - |
GRCh38 GRCh38 GRCh37 |
40 | 57 | |
DCST1 | - | - | - |
GRCh38 GRCh37 |
36 | 76 |
DCST2 | - | - | - |
GRCh38 GRCh37 |
81 | 98 |
DPM3 | - | - |
GRCh38 GRCh37 |
64 | 85 | |
EFNA1 | - | - |
GRCh38 GRCh37 |
11 | 27 | |
EFNA3 | - | - |
GRCh38 GRCh37 |
- | 32 | |
EFNA4 | - | - |
GRCh38 GRCh37 |
- | 47 | |
FAM189B | - | - |
GRCh38 GRCh38 GRCh37 |
- | - |
There are 15 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) |
|
Sep 24, 2018 | RCV001005143.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022