ClinVar Genomic variation as it relates to human health
GRCh37/hg19 21q22.2(chr21:39892114-40905632)x1
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 | |||
BRWD1 | - | - |
GRCh38 GRCh37 |
163 | 241 | |
ERG | - | - |
GRCh38 GRCh37 |
27 | 102 | |
ETS2 | - | - |
GRCh38 GRCh37 |
27 | 109 | |
GET1 | - | - |
GRCh38 GRCh37 |
- | 133 | |
HMGN1 | - | - |
GRCh38 GRCh37 |
9 | 81 | |
LCA5L | - | - | - |
GRCh38 GRCh37 |
- | 117 |
LINC00114 | - | - |
GRCh38 GRCh37 |
1 | 74 | |
PSMG1 | - | - |
GRCh38 GRCh37 |
19 | 91 | |
SH3BGR | - | - |
GRCh38 GRCh37 |
- | 97 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Mar 1, 2021 | RCV001836600.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 17, 2022