ClinVar Genomic variation as it relates to human health
GRCh38/hg38 22q13.1(chr22:38957661-39011489)x1
Germline
Classification
(1)
Benign
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 | |||
APOBEC3A | - | - |
GRCh38 GRCh37 |
9 | 34 | |
APOBEC3B | - | - |
GRCh38 GRCh37 |
18 | 50 | |
APOBEC3B-AS1 | - | - | - | GRCh38 | - | 13 |
LOC126863151 | - | - | - | GRCh38 | - | 8 |
LOC130067442 | - | - | - | GRCh38 | - | 9 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Benign (1) |
|
Oct 1, 2010 | RCV000142694.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024