ClinVar Genomic variation as it relates to human health
GRCh37/hg19 3q13.13-13.2(chr3:110719980-111389974)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 | |||
CD96 | - | - |
GRCh38 GRCh37 |
117 | 152 | |
NECTIN3 | - | - |
GRCh38 GRCh37 |
28 | 45 | |
NECTIN3-AS1 | - | - | - |
GRCh38 GRCh37 |
- | 17 |
ZBED2 | - | - |
GRCh38 GRCh37 |
- | 35 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 17, 2017 | RCV000682295.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022