ClinVar Genomic variation as it relates to human health
GRCh37/hg19 4p16.3(chr4:68345-694966)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 | |||
ATP5ME | - | - |
GRCh38 GRCh37 |
7 | 165 | |
MYL5 | - | - |
GRCh38 GRCh37 |
- | 173 | |
PDE6B | - | - |
GRCh38 GRCh37 |
970 | 1258 | |
PIGG | - | - |
GRCh38 GRCh37 |
988 | 1158 | |
SLC49A3 | - | - | - |
GRCh38 GRCh37 |
48 | 222 |
ZNF141 | - | - |
GRCh38 GRCh37 |
42 | 202 | |
ZNF595 | - | - | - |
GRCh38 GRCh37 |
33 | 185 |
ZNF718 | - | - | - |
GRCh38 GRCh37 |
6 | 167 |
ZNF721 | - | - | - |
GRCh38 GRCh37 |
81 | 258 |
ZNF732 | - | - | - |
GRCh38 GRCh37 |
46 | 199 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Dec 6, 2017 | RCV000847202.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022