Annotation Detail
Information
- Associated Genes
- GBA1 LOC106627981
- Associated Variants
-
GBA1 p.Arg502His (p.R502H)
(
ENST00000428024.3,
ENST00000327247.9,
ENST00000368373.8,
ENST00000427500.7 )
GBA1 p.Arg502His (p.R502H) ( ENST00000327247.9, ENST00000368373.8, ENST00000427500.7, ENST00000428024.3 ) - Associated Disease
- Gaucher disease type I
- Source Database
- ClinVar
- Description
- NM_000157.4(GBA1):c.1505G>A (p.Arg502His) AND Gaucher disease type I
- ClinVar Allele ID
- 33922
- ClinVar RefSeq Alternation Syntax
- NM_001005742.3:c.1505G>A
- ClinVar RefSeq Alternation Syntax
- NM_001171811.2:c.1244G>A
- ClinVar RefSeq Alternation Syntax
- NM_000157.4:c.1505G>A
- ClinVar RefSeq Alternation Syntax
- NM_001005741.3:c.1505G>A
- ClinVar RefSeq Alternation Syntax
- NM_001171812.2:c.1358G>A
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2020-01-22
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000409564
- ClinVar Disease
- Gaucher disease type I
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs