rs7613875
▶GWAS Catalog Trait Associations (5)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (5)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
creativity measurement
Kim H et al. “Genome-wide association analyses using machine learning-based phenotyping reveal genetic architecture of occupational creativity and overlap with psychiatric disorders.” Psychiatry Research 333:115753 (2024)
Allele C
OR 0.03
p 9.0e-19
N 241,736
Large GWAS
European
body mass index
Hoffmann TJ et al. “A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci.” Genetics 210(2):499-515 (2018)
Allele C
OR —
β 0.020
p 7.0e-14
N 334,487
Large GWAS
multi-ancestry
Winkler TW et al. “The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.” Plos Genetics 11(10):e1005378 (2015)
Allele C
OR —
β 0.016
p 1.0e-8
N 309,889
Large GWAS
European
Akiyama M et al. “Genome-wide association study identifies 112 new loci for body mass index in the Japanese population.” Nature Genetics 49(10):1458-1467 (2017)
Allele C
OR 0.02
p 4.0e-9
N 158,284
Large GWAS
multi-ancestry
non-alcoholic fatty liver disease
Du M et al. “Cross-trait genomic modeling reveals the polygenic architecture and systemic impact of MASLD.” Science Advances 12(7):eaeb5665 (2026)
Allele C
OR 0.03
p 2.0e-13
N 122,644
Large GWAS
European
dental caries
Nogawa S et al. “Genome-wide association meta-analysis identifies two novel loci associated with dental caries.” Bmc Oral Health 24(1):1003 (2024)
Allele A
OR 6.04
p 1.0e-9
N 533,348
Meta-analysisLarge GWAS
multi-ancestry
gastroesophageal reflux disease
An J et al. “Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.” Nature Communications 10(1):4219 (2019)
Allele A
OR 1.03
p 3.0e-8
N 385,276
Large GWAS
European, NR
This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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