rs10512344 - LINC01505
Magnitude 2.2 · 1 study on file
Reported associations
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Female-specific Association Between Variants on Chromosome 9 and Self-reported Diagnosis of Irritable Bowel Syndrome - Unknown journal (n.d.) · Unknown authors · PubMed 29626450
ABSTRACT: Background & Aims Genetic factors are believed to affect risk for irritable bowel syndrome (IBS), but there have been no sufficiently powered and adequately sized studies. To identify DNA variants associated with IBS risk, we performed a genome-wide association study (GWAS) of the large UK Biobank population-based cohort, which includes genotype and health data from 500,000 participants. Methods We studied 7,287,191 high-quality single-nucleotide polymorphisms in individuals who self-reported a doctor's diagnosis of IBS (cases; m=9576) compared to the remainder of the cohort (controls; n=336,499) (mean age of study subjects, 40-69 years). Genome-wide significant findings were further investigated in 2045 patients with IBS from tertiary centers and 7955 population controls fro
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Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Screening
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Monitor for IBS-constipation symptoms High
rs10512344 C allele shows female-specific genetic risk for IBS-C phenotype (p=4.29e-10 in females), with association to harder stools and constipation
Track bowel frequency and stool consistency; report persistent changes to healthcare provider for IBS evaluation