ClinVar Genomic variation as it relates to human health
GRCh37/hg19 18q12.2(chr18:32988821-33701451)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 | |||
C18orf21 | - | - | - |
GRCh38 GRCh37 |
- | 44 |
GALNT1 | - | - |
GRCh38 GRCh37 |
9 | 51 | |
INO80C | - | - | - |
GRCh38 GRCh37 |
15 | 59 |
MIR187 | - | - |
GRCh38 GRCh37 |
- | 43 | |
RPRD1A | - | - |
GRCh38 GRCh37 |
7 | 54 | |
SLC39A6 | - | - |
GRCh38 GRCh37 |
39 | 86 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Mar 14, 2018 | RCV000684010.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023