ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11p15.4(chr11:8859352-9226956)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 | |||
AKIP1 | - | - |
GRCh38 GRCh37 |
1 | 19 | |
ASCL3 | - | - |
GRCh38 GRCh37 |
14 | 33 | |
C11orf16 | - | - | - |
GRCh38 GRCh37 |
4 | 22 |
DENND2B | - | - |
GRCh38 GRCh37 |
83 | 106 | |
DENND5A | - | - |
GRCh38 GRCh37 |
523 | 586 | |
NRIP3 | - | - |
GRCh38 GRCh37 |
14 | 32 | |
SCUBE2 | - | - |
GRCh38 GRCh37 |
17 | 85 | |
TMEM9B | - | - | - |
GRCh38 GRCh37 |
5 | 26 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Dec 28, 2018 | RCV001006386.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022