ClinVar Genomic variation as it relates to human health
GRCh37/hg19 14q24.3(chr14:76082940-78372356)x1
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 | |||
ADCK1 | - | - |
GRCh38 GRCh37 |
30 | 54 | |
AHSA1 | - | - |
GRCh38 GRCh37 |
13 | 35 | |
ALKBH1 | - | - |
GRCh38 GRCh37 |
22 | 49 | |
ANGEL1 | - | - |
GRCh38 GRCh37 |
43 | 64 | |
C14orf178 | - | - | - |
GRCh38 GRCh37 |
- | 24 |
CIPC | - | - |
GRCh38 GRCh37 |
26 | 41 | |
ERG28 | - | - |
GRCh38 GRCh37 |
1 | 22 | |
ESRRB | - | - |
GRCh38 GRCh37 |
250 | 273 | |
FLVCR2 | - | - |
GRCh38 GRCh37 |
141 | 212 | |
GPATCH2L | - | - | - |
GRCh38 GRCh37 |
18 | 35 |
There are 19 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 |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Aug 22, 2014 | RCV000511668.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024