ClinVar Genomic variation as it relates to human health
NM_012179.4(FBXO7):c.520T>A (p.Ser174Thr)
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
FBXO7 | - | - |
GRCh38 GRCh37 |
410 | 429 |
Conditions - Germline
There are no conditions for this variant because no interpretation for the single variant has been submitted to ClinVar yet.
Citations for germline classification of this variant
HelpConditions - Somatic
There are no conditions for this variant because no interpretation for the single variant has been submitted to ClinVar yet.
Citations for somatic classification of this variant
HelpText-mined citations for rs1458349518 ...
HelpRecord last updated Apr 15, 2024