ClinVar Genomic variation as it relates to human health
GRCh37/hg19 10q24.32(chr10:103197122-103601973)x3
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
BTRC | No evidence available | No evidence available |
GRCh38 GRCh37 |
73 | 132 | |
FBXW4 | No evidence available | No evidence available |
GRCh38 GRCh37 |
71 | 150 | |
POLL | No evidence available | No evidence available |
GRCh38 GRCh37 |
60 | 113 | |
DPCD | - | - |
GRCh38 GRCh37 |
15 | 72 | |
FGF8 | - | - |
GRCh38 GRCh37 |
98 | 122 | |
KCNIP2 | - | - |
GRCh38 GRCh37 |
4 | 30 | |
NPM3 | - | - |
GRCh38 GRCh37 |
13 | 34 | |
OGA | - | - |
GRCh38 GRCh37 |
31 | 51 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
- | RCV003986886.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 30, 2024