rs3130968
This is a intergenic variant variant.
▶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.
Raynaud disease
Tervi A et al. “Genetic and functional analysis of Raynaud's syndrome implicates loci in vasculature and immunity.” Cell Genomics 4(9):100630 (2024)
Allele T
OR 0.16
p 7.0e-16
N 1,118,229
Large GWAS
European
peripheral arterial disease
van Zuydam NR et al. “Genome-Wide Association Study of Peripheral Artery Disease.” Circulation. Genomic and Precision Medicine 14(5):e002862 (2021)
Allele T
OR 1.07
p 3.0e-12
N 461,634
Large GWAS
multi-ancestry
Klarin D et al. “Genome-wide association study of peripheral artery disease in the Million Veteran Program.” Nature Medicine 25(8):1274-1279 (2019)
Allele T
OR 1.07
p 3.0e-10
N 243,060
Major Consortium StudyLarge GWAS
multi-ancestry
forced expiratory volume, 25-hydroxyvitamin D3 measurement
Seo J et al. “Exploiting meta-analysis of genome-wide interaction with serum 25-hydroxyvitamin D to identify novel genetic loci associated with pulmonary function.” The American Journal of Clinical Nutrition 119(5):1227-1237 (2024)
Allele C
OR —
p 1.0e-9
N 95,952
Meta-analysisLarge GWAS
multi-ancestry
BMI-adjusted waist-hip ratio
Christakoudi S et al. “GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer.” Scientific Reports 11(1):10688 (2021)
Allele T
OR 0.02
p 4.0e-9
N 219,872
Major Consortium StudyLarge GWAS
European
BMI-adjusted waist circumference
Christakoudi S et al. “GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer.” Scientific Reports 11(1):10688 (2021)
Allele T
OR 0.02
p 7.0e-9
N 219,872
Major Consortium StudyLarge GWAS
European
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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