ClinVar Genomic variation as it relates to human health
NM_173651.4(FSIP2):c.5453C>T (p.Thr1818Ile)
Germline
Classification
(1)
Likely benign
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 | |||
FSIP2 | - | - |
GRCh38 GRCh37 |
334 | 701 | |
FSIP2-AS1 | - | - | - | GRCh38 | - | 328 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Jan 4, 2024 | RCV004387134.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024