Annotation Detail
Information
- Associated Genes
- LDLR
- Associated Variants
-
LDLR p.Asn591= (p.N591=)
(
ENST00000252444.10,
ENST00000455727.6,
ENST00000535915.5,
ENST00000545707.5,
ENST00000557933.5,
ENST00000558013.5,
ENST00000558518.6,
ENST00000560467.2 )
LDLR p.Asn591= (p.N591=) ( ENST00000252444.10, ENST00000455727.6, ENST00000535915.5, ENST00000545707.5, ENST00000557933.5, ENST00000558013.5, ENST00000558518.6, ENST00000560467.2 ) - Associated Disease
- Hypercholesterolemia, familial, 1
- Source Database
- ClinVar
- Description
- NM_000527.5(LDLR):c.1773C>T (p.Asn591=) AND Hypercholesterolemia, familial, 1
- ClinVar Allele ID
- 198016
- ClinVar RefSeq Alternation Syntax
- NM_000527.5:c.1773C>T
- ClinVar RefSeq Alternation Syntax
- NM_001195799.2:c.1650C>T
- ClinVar RefSeq Alternation Syntax
- NM_001195798.2:c.1773C>T
- ClinVar RefSeq Alternation Syntax
- NM_001195800.2:c.1269C>T
- ClinVar RefSeq Alternation Syntax
- NM_001195803.2:c.1392C>T
- Clinical Significance Description
- Benign/Likely benign
- Clinical Significance Last Update
- 2023-03-30
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000237654
- ClinVar Disease
- Hypercholesterolemia, familial, 1
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs