Variant (rsID / SNP)
rs187831231
rs187831231 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCARB1. Location: chromosome 12, position 125,298,855. Clinical significance in the table: association.
Reference-table entries
SCARB1Association
- Clinical significance (as recorded)
- association
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:125298855
- Cytoband
- 12q24.31
- HGVS
- NM_005505.5(SCARB1):c.523A>G (p.Thr175Ala)
- Allele change
- Missense_T175A
Associated conditions / phenotypes
High density lipoprotein cholesterol level quantitative trait locus 6
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.