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CELSR2 and familial hypercholesterolemia are reported together in 1 article.
Gene
CELSR2
- HGNC
- HGNC:3231
5articles
5mentions
4variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
Phenotype
Familial hypercholesterolemia
- HPO
- HP:0003124
- OMIM
- 143890
165articles
165mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
1 records shown · first 60Association of CELSR2, APOB100, ABCG5/8, LDLR, and APOE polymorphisms and their genetic risks with lipids among the Thai subjects.
PMID 36619676 | PMCID PMC9812717 | DOI 10.1016/j.sjbs.2022.103554 · Saudi journal of biological sciences · 2023 · 11 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | CELSR2 | “Association of CELSR2, APOB100, ABCG5/8, LDLR, and APOE polymorphisms and their genetic risks with lipids among the Thai subjects.” | 0.98 | hgnc_dict_v1 |
| phenotype | familial hypercholesterolemia | “BACKGROUND: Hypercholesterolemia is a common cardiovascular risk factor.” | 0.93 | phenotype_alias_lexicon_v2 |
| gene | ABCG5 | “Association of CELSR2, APOB100, ABCG5/8, LDLR, and APOE polymorphisms and their genetic risks with lipids among the Thai subjects.” | 0.98 | hgnc_dict_v1 |
| gene | LDLR | “Association of CELSR2, APOB100, ABCG5/8, LDLR, and APOE polymorphisms and their genetic risks with lipids among the Thai subjects.” | 0.98 | hgnc_dict_v1 |