ClinVar Genomic variation as it relates to human health
GRCh37/hg19 19q13.12(chr19:35613953-36183886)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 | |||
ATP4A | - | - |
GRCh38 GRCh37 |
140 | 159 | |
CD22 | - | - |
GRCh38 GRCh37 |
57 | 82 | |
COX6B1 | - | - |
GRCh38 GRCh37 |
52 | 72 | |
DMKN | - | - |
GRCh38 GRCh37 |
7 | 26 | |
ETV2 | - | - |
GRCh38 GRCh37 |
19 | 50 | |
FAM187B | - | - | - |
GRCh38 GRCh37 |
39 | 59 |
FFAR1 | - | - |
GRCh38 GRCh37 |
24 | 44 | |
FFAR2 | - | - |
GRCh38 GRCh37 |
32 | 50 | |
FFAR3 | - | - |
GRCh38 GRCh37 |
37 | 57 | |
FXYD1 | - | - |
GRCh38 GRCh37 |
3 | 23 |
There are 16 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Aug 22, 2018 | RCV000845987.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022