ClinVar Genomic variation as it relates to human health
NM_006796.3(AFG3L2):c.2375dup (p.Gly792_Glu793insTer)
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
AFG3L2 | - | - |
GRCh38 GRCh37 |
416 | 553 | |
TUBB6 | - | - |
GRCh38 GRCh37 |
30 | 166 |
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 rs1907449398 ...
HelpRecord last updated Jul 15, 2024