ClinVar Genomic variation as it relates to human health
GRCh37/hg19 10q23.33(chr10:95234481-95431148)x1
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 | |||
CEP55 | - | - |
GRCh38 GRCh37 |
83 | 108 | |
FFAR4 | - | - |
GRCh38 GRCh37 |
28 | 56 | |
FRA10AC1 | - | - |
GRCh38 GRCh37 |
23 | 53 | |
MYOF | - | - |
GRCh38 GRCh37 |
206 | 231 | |
PDE6C | - | - |
GRCh38 GRCh37 |
652 | 680 | |
RBP4 | - | - |
GRCh38 GRCh37 |
167 | 195 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 7, 2018 | RCV001006347.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022