ClinVar Genomic variation as it relates to human health
NM_020919.4(ALS2):c.3624+5G>C
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
ALS2 | - | - |
GRCh38 GRCh37 |
996 | 1040 |
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 rs386134186 ...
HelpRecord last updated May 12, 2024