ClinVar Genomic variation as it relates to human health
GRCh37/hg19 3q27.3(chr3:186149060-186599706)
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 | |||
ADIPOQ | - | - |
GRCh38 GRCh37 |
- | 68 | |
AHSG | - | - |
GRCh38 GRCh37 |
51 | 92 | |
CRYGS | - | - |
GRCh38 GRCh37 |
49 | 92 | |
DNAJB11 | - | - |
GRCh38 GRCh37 |
118 | 169 | |
EIF4A2 | - | - |
GRCh38 GRCh37 |
37 | 84 | |
FETUB | - | - |
GRCh38 GRCh37 |
13 | 72 | |
HRG | - | - |
GRCh38 GRCh37 |
75 | 130 | |
KNG1 | - | - |
GRCh38 GRCh37 |
67 | 109 | |
RFC4 | - | - |
GRCh38 GRCh37 |
22 | 69 | |
SNORA63 | - | - |
GRCh38 GRCh37 |
- | 46 |
There are 2 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Mar 1, 2022 | RCV002053397.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 16, 2022