ClinVar Genomic variation as it relates to human health
GRCh37/hg19 1q32.1(chr1:205364836-205697334)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 | |||
CDK18 | - | - |
GRCh38 GRCh37 |
36 | 54 | |
ELK4 | - | - |
GRCh38 GRCh37 |
22 | 41 | |
LEMD1 | - | - |
GRCh38 GRCh37 |
11 | 32 | |
MFSD4A | - | - | - |
GRCh38 GRCh37 |
4 | 23 |
NUCKS1 | - | - |
GRCh38 GRCh37 |
6 | 24 | |
SLC45A3 | - | - |
GRCh38 GRCh37 |
32 | 53 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jan 10, 2018 | RCV000684690.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022