ClinVar Genomic variation as it relates to human health
NM_213720.3(CHCHD10):c.43C>A (p.Arg15Ser)
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
CHCHD10 | - | - |
GRCh38 GRCh38 GRCh37 |
233 | 345 |
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 rs730880032 ...
HelpRecord last updated Jan 26, 2024