ClinVar Genomic variation as it relates to human health
NM_000295.5(SERPINA1):c.602A>G (p.Asp201Gly)
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
SERPINA1 | - | - |
GRCh38 GRCh38 GRCh37 |
470 | 505 |
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 rs1555368976 ...
HelpRecord last updated May 01, 2024