rs477895

This is a upstream gene variant variant in the BAD gene.

GWAS Catalog Trait Associations (6)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

platelet count

Allele T
OR
p 8.0e-23
N 721,201
Large GWAS
multi-ancestry
Allele T
OR 4.19
p 5.0e-8
N 16,388
Meta-analysisLarge GWAS
African American or Afro-Caribbean

hip circumference

Allele T
OR 0.02
p 9.0e-17
N 394,642
Large GWAS
European

fat pad mass

Allele T
OR 0.02
p 1.0e-13
N 394,642
Large GWAS
European

body fat percentage

Allele T
OR 0.01
p 4.0e-13
N 394,642
Large GWAS
European

body weight

Allele T
OR 0.02
p 5.0e-13
N 394,642
Large GWAS
European
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 0.01
p 2.0e-8
N 525,535
Large GWAS
multi-ancestry

body mass index

Allele T
OR 0.02
p 2.0e-12
N 394,642
Large GWAS
European
Sidorenko J et al. Genetic architecture reconciles linkage and association studies of complex traits. Nature Genetics 56(11):2352-2360 (2024)
Allele T
OR 0.02
p 2.0e-11
N 650,000
Large GWAS
European

About BAD

The protein encoded by this gene is a member of the BCL-2 family. BCL-2 family members are known to be regulators of programmed cell death. This protein positively regulates cell apoptosis by forming heterodimers with BCL-xL (B-cell lymphoma-extra large) and BCL-2, and reversing their death repressor activity. Proapoptotic activity of this protein is regulated through its phosphorylation. Protein kinases AKT and MAP kinase, as well as protein phosphatase calcineurin were found to be involved in the regulation of this protein. Alternative splicing of this gene results in two transcript variants which encode the same isoform. [provided by RefSeq, Dec 2019]

View all BAD variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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