ClinVar Genomic variation as it relates to human health
GRCh37/hg19 3q25.32-25.33(chr3:157991657-159073531)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 | |||
GFM1 | - | - |
GRCh38 GRCh37 |
864 | 915 | |
IQCJ | - | - |
GRCh38 GRCh37 |
- | 43 | |
IQCJ-SCHIP1 | - | - | - |
GRCh38 GRCh37 |
- | 73 |
LXN | - | - |
GRCh38 GRCh37 |
- | 49 | |
MFSD1 | - | - | - |
GRCh38 GRCh37 |
37 | 68 |
MLF1 | - | - |
GRCh38 GRCh37 |
22 | 49 | |
RARRES1 | - | - |
GRCh38 GRCh37 |
17 | 59 | |
RSRC1 | - | - |
GRCh38 GRCh37 |
42 | 71 | |
SCHIP1 | - | - |
GRCh38 GRCh37 |
- | 57 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Apr 18, 2018 | RCV000682320.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022