ClinVar Genomic variation as it relates to human health
GRCh38/hg38 6p25.1(chr6:5315620-5695253)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 | |||
FARS2 | - | - |
GRCh38 GRCh37 |
321 | 602 | |
FARS2-AS1 | - | - | - | GRCh38 | - | 24 |
LOC101927950 | - | - | - | GRCh38 | - | 26 |
LOC126859565 | - | - | - | GRCh38 | - | 206 |
LOC126859566 | - | - | - | GRCh38 | - | 24 |
LOC126859567 | - | - | - | GRCh38 | - | 24 |
LOC126859568 | - | - | - | GRCh38 | - | 25 |
LOC129389433 | - | - | - | GRCh38 | - | 24 |
LOC129995678 | - | - | - | GRCh38 | - | 26 |
LOC129995679 | - | - | - | GRCh38 | - | 24 |
There are 2 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Sep 17, 2012 | RCV000139014.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024