rs1034471848 (LINC03142): non-newborn jaundice
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Key takeaways
- rs1034471848 is linked to non-newborn jaundice
- The effect allele T increases risk in about 628 thousand people
- Reported effect size 2.77 p=2e-14
Key takeaways
- rs1034471848 is linked to non-newborn jaundice
- The effect allele T increases risk in about 628 thousand people
- Reported effect size 2.77 p=2e-14
What the research says This variant is associated with Jaundice (not of newborn) PheCode 573.5 PMID 39024449. The effect allele T increases risk in about 628 thousand individuals with a reported effect size of 2.77 p=2e-14 PMID 39024449.
Reported associations
- Jaundice (not of newborn) the variant increases risk with a reported effect size 2.77 p=2e-14 PMID 39024449.
Evidence quality The evidence comes from a genome-wide association study involving about 628 thousand individuals and reports an effect allele T associated with Jaundice (not of newborn) PheCode 573.5 with a reported effect size of 2.77 p=2e-14 [PMID 39024449]. No other studies are provided so replication is not addressed.
No lifestyle considerations on file for this variant.
Frequently asked questions
What does rs1034471848 mean?
It is a genetic variant at the LINC03142 locus that has been linked to non-newborn jaundice in large studies.
Is this variant related to newborn jaundice?
No it is specifically associated with Jaundice not of newborn as indicated by PheCode 573.5.
How strong is the link between rs1034471848 and Jaundice?
The study reports an effect size of 2.77 p=2e-14 indicating a very strong association in about 628 thousand individuals.