ClinVar Genomic variation as it relates to human health
GRCh38/hg38 3q22.3(chr3:137593514-138443019)x3
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 | |||
A4GNT | - | - |
GRCh38 GRCh37 |
23 | 45 | |
ARMC8 | - | - |
GRCh38 GRCh37 |
17 | 46 | |
CLDN18 | - | - |
GRCh38 GRCh37 |
18 | 37 | |
DBR1 | - | - |
GRCh38 GRCh37 |
156 | 197 | |
DZIP1L | - | - |
GRCh38 GRCh37 |
209 | 230 | |
ESYT3 | - | - |
GRCh38 GRCh37 |
71 | 101 | |
LINC01210 | - | - | - | GRCh38 | - | 11 |
LOC108281117 | - | - | - | GRCh38 | - | 14 |
LOC110120785 | - | - | - | GRCh38 | - | 11 |
LOC129389141 | - | - | - | GRCh38 | - | 14 |
There are 8 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Aug 12, 2011 | RCV000051534.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024