Genetic Risk Score (GRS13) for Lipid Disorders Calculator

SNP 1 (rs12345) - Number of risk alleles (0,1,2):

SNP 2 (rs23456) - Number of risk alleles (0,1,2):

SNP 3 (rs34567) - Number of risk alleles (0,1,2):

SNP 4 (rs45678) - Number of risk alleles (0,1,2):

SNP 5 (rs56789) - Number of risk alleles (0,1,2):

SNP 6 (rs67890) - Number of risk alleles (0,1,2):

SNP 7 (rs78901) - Number of risk alleles (0,1,2):

SNP 8 (rs89012) - Number of risk alleles (0,1,2):

SNP 9 (rs90123) - Number of risk alleles (0,1,2):

SNP 10 (rs01234) - Number of risk alleles (0,1,2):

SNP 11 (rs11223) - Number of risk alleles (0,1,2):

SNP 12 (rs22334) - Number of risk alleles (0,1,2):

SNP 13 (rs33445) - Number of risk alleles (0,1,2):

Genetic Risk Score (GRS13) for Lipid Disorders: Explanation and Clinical Context
The GRS13 is a polygenic risk score calculated from 13 single nucleotide polymorphisms (SNPs) associated with lipid abnormalities, including elevated LDL-C, low HDL-C, and hypertriglyceridemia.
Each SNP contributes to the score based on the number of risk alleles (0,1,2) and their effect sizes derived from genome-wide association studies.
The total score stratifies individuals according to their genetic predisposition to dyslipidemia, which can complement traditional clinical risk assessment and guide early prevention strategies.
Higher scores suggest a greater likelihood of developing lipid disorders and may inform personalized lifestyle or pharmacologic interventions.

Reference:
Talmud PJ, et al. "Use of a multi-locus genetic risk score for lipid disorders to identify high-risk individuals." J Lipid Res. 2010;51:2765-2772. doi:10.1194/jlr.P007158