Annotation Detail
Information
- Associated Genes
- SMPD1
- Associated Variants
-
SMPD1 c.1092-1G>C
(
ENST00000342245.9,
ENST00000527275.5 )
SMPD1 c.1092-1G>C ( ENST00000342245.9, ENST00000527275.5 ) - Associated Disease
- Niemann-Pick disease, type A
- Source Database
- ClinVar
- Description
- NM_000543.5(SMPD1):c.1092-1G>C AND Niemann-Pick disease, type A
- ClinVar Allele ID
- 99219
- ClinVar RefSeq Alternation Syntax
- NM_000543.5:c.1092-1G>C
- ClinVar RefSeq Alternation Syntax
- NM_001318088.2:c.171-1G>C
- ClinVar RefSeq Alternation Syntax
- NM_001007593.3:c.1089-1G>C
- ClinVar RefSeq Alternation Syntax
- NM_001318087.2:c.1092-1G>C
- ClinVar RefSeq Alternation Syntax
- NM_001365135.2:c.1132-402G>C
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2020-12-09
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000410331
- ClinVar Disease
- Niemann-Pick disease, type A
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs