ClinVar Genomic variation as it relates to human health
NM_022166.4(XYLT1):c.1793G>A (p.Arg598His)
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 | |||
LOC102723692 | - | - | - |
GRCh38 GRCh38 |
- | 139 |
XYLT1 | - | - |
GRCh38 GRCh38 GRCh37 |
409 | 626 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Aug 26, 2022 | RCV002766207.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 06, 2024