ClinVar Genomic variation as it relates to human health
NM_022787.4(NMNAT1):c.275G>A (p.Trp92Ter)
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
NMNAT1 | - | - |
GRCh38 GRCh37 |
198 | 245 |
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 rs1641792929 ...
HelpRecord last updated Jun 23, 2024