ClinVar Genomic variation as it relates to human health
GRCh37/hg19 8q24.12-24.13(chr8:121938227-125485728)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 | |||
ANXA13 | - | - |
GRCh38 GRCh37 |
28 | 80 | |
ATAD2 | - | - |
GRCh38 GRCh37 |
69 | 118 | |
C8orf76 | - | - | - |
GRCh38 GRCh37 |
- | 51 |
DERL1 | - | - |
GRCh38 GRCh37 |
10 | 62 | |
FAM83A | - | - | - |
GRCh38 GRCh37 |
24 | 73 |
FAM91A1 | - | - | - |
GRCh38 GRCh37 |
31 | 83 |
FBXO32 | - | - |
GRCh38 GRCh37 |
31 | 85 | |
FER1L6 | - | - | - |
GRCh38 GRCh37 |
38 | 169 |
HAS2 | - | - |
GRCh38 GRCh37 |
14 | 64 | |
HAS2-AS1 | - | - |
GRCh38 GRCh37 |
- | 50 |
There are 8 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) |
|
Nov 12, 2020 | RCV001281354.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023