ClinVar Genomic variation as it relates to human health
GRCh37/hg19 16q24.3(chr16:89337891-90155062)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 | |||
ANKRD11 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
2420 | 2584 | |
TUBB3 | No evidence available | No evidence available |
GRCh38 GRCh37 |
288 | 354 | |
CDK10 | - | - |
GRCh38 GRCh37 |
83 | 159 | |
CENPBD1 | - | - | - |
GRCh38 GRCh37 |
14 | 67 |
CHMP1A | - | - |
GRCh38 GRCh37 |
198 | 274 | |
CPNE7 | - | - |
GRCh38 GRCh37 |
66 | 137 | |
DBNDD1 | - | - | - |
GRCh38 GRCh37 |
16 | 69 |
DEF8 | - | - | - |
GRCh38 GRCh37 |
40 | 94 |
DPEP1 | - | - |
GRCh38 GRCh37 |
19 | 92 | |
FANCA | - | - |
GRCh38 GRCh37 |
4077 | 5203 |
There are 13 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Apr 1, 2021 | RCV001827759.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022