ClinVar Genomic variation as it relates to human health
GRCh37/hg19 19q13.12(chr19:35548527-35772471)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 | |||
FAM187B | - | - | - |
GRCh38 GRCh37 |
39 | 59 |
FXYD1 | - | - |
GRCh38 GRCh37 |
3 | 23 | |
FXYD3 | - | - |
GRCh38 GRCh37 |
14 | 36 | |
FXYD5 | - | - |
GRCh38 GRCh37 |
10 | 36 | |
FXYD7 | - | - |
GRCh38 GRCh37 |
2 | 22 | |
HPN | - | - |
GRCh38 GRCh37 |
7 | 40 | |
LGI4 | - | - |
GRCh38 GRCh37 |
103 | 125 | |
LSR | - | - |
GRCh38 GRCh37 |
124 | 145 | |
USF2 | - | - |
GRCh38 GRCh37 |
20 | 47 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jun 15, 2018 | RCV000848432.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022