ClinVar Genomic variation as it relates to human health
GRCh37/hg19 16q24.2-24.3(chr16:88222732-90155062)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 | |
CDH15 | No evidence available | No evidence available |
GRCh38 GRCh37 |
235 | 349 | |
TUBB3 | No evidence available | No evidence available |
GRCh38 GRCh37 |
288 | 354 | |
ACSF3 | - | - |
GRCh38 GRCh37 |
858 | 1052 | |
APRT | - | - |
GRCh38 GRCh37 |
130 | 243 | |
CBFA2T3 | - | - |
GRCh38 GRCh37 |
44 | 142 | |
CDK10 | - | - |
GRCh38 GRCh37 |
83 | 159 | |
CDT1 | - | - |
GRCh38 GRCh37 |
388 | 489 | |
CENPBD1 | - | - | - |
GRCh38 GRCh37 |
14 | 67 |
CHMP1A | - | - |
GRCh38 GRCh37 |
198 | 274 |
There are 33 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) |
|
Jan 13, 2020 | RCV001258663.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023