Disease Control group group Allele A 25,350 24,133 Allele C Allele C 24,650 25,867 Allele T SNP1 SNP 2; risk allele is C SNP 3; risk allele is G SNP 2; risk allele is T SNP 3; risk allele is A Results are shown above for 3 biallelic SNPs on the same chromosome used in a GWAS examining SNP-trait correlations for a complex human disease trait. Table entries show the number of people with the indicated SNP allele that have the disease (disease group) or don't have the disease (control group). Which SNP would have the highest -log₁0 (p-value) score in a Manhattan plot summarizing results of this GWAS, and which is the SNP "risk allele"? SNP 1; risk allele is A SNP2 SNP 1; risk allele is C Disease Control group group 1,420 1,509 48,580 48,491 SNP3 Allele G Allele A Disease Control group group 47,360 3,109 2,640 46,891
Disease Control group group Allele A 25,350 24,133 Allele C Allele C 24,650 25,867 Allele T SNP1 SNP 2; risk allele is C SNP 3; risk allele is G SNP 2; risk allele is T SNP 3; risk allele is A Results are shown above for 3 biallelic SNPs on the same chromosome used in a GWAS examining SNP-trait correlations for a complex human disease trait. Table entries show the number of people with the indicated SNP allele that have the disease (disease group) or don't have the disease (control group). Which SNP would have the highest -log₁0 (p-value) score in a Manhattan plot summarizing results of this GWAS, and which is the SNP "risk allele"? SNP 1; risk allele is A SNP2 SNP 1; risk allele is C Disease Control group group 1,420 1,509 48,580 48,491 SNP3 Allele G Allele A Disease Control group group 47,360 3,109 2,640 46,891
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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Step 1: About GWAS
In a Genome-Wide Association Study (GWAS), the -log10(p-value) score for each SNP (Single Nucleotide Polymorphism) measures its statistical significance in association with a particular disease trait. The higher the -log10(p-value) score, the more significant the association between the SNP and the disease.
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