ClinVar Genomic variation as it relates to human health
GRCh38/hg38 16p13.3(chr16:350651-396961)x4
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 | |||
AXIN1 | - | - |
GRCh38 GRCh37 |
82 | 151 | |
LOC100134368 | - | - | - | GRCh38 | - | 18 |
LOC130058093 | - | - | - | GRCh38 | - | 18 |
LOC130058094 | - | - | - | GRCh38 | - | 18 |
LOC130058095 | - | - | - | GRCh38 | - | 18 |
LOC130058096 | - | - | - | GRCh38 | - | 18 |
LOC130058097 | - | - | - | GRCh38 | - | 18 |
LOC130058098 | - | - | - | GRCh38 | - | 18 |
LOC130058099 | - | - | - | GRCh38 | - | 18 |
LOC130058100 | - | - | - | GRCh38 | - | 18 |
There are 3 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Nov 30, 2010 | RCV000134454.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023