ClinVar Genomic variation as it relates to human health
NM_005458.8(GABBR2):c.1236+11101=
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
GABBR2 | - | - |
GRCh38 GRCh37 |
920 | 1002 |
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 rs2491397 ...
HelpRecord last updated Aug 11, 2024