rs202200760

This is a protein-altering variant in the NR2F6 gene.

GWAS Catalog Trait Associations (3)

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

hypogonadism

Allele G
OR 0.13
p 2.0e-11
N 145,389
Major Consortium StudyLarge GWAS
multi-ancestry

sex hormone-binding globulin measurement

Allele C
OR 0.17
p 8.0e-81
N 196,901
Large GWAS
European
Allele C
OR 0.08
p 5.0e-120
N 188,908
Large GWAS
European
Allele C
OR 0.11
p 2.0e-17
N 47,745
Large GWAS
European
Allele C
OR 5.63
p 1.0e-9
N 36,203
Major Consortium StudyLarge GWAS
European
Allele C
OR 0.18
p 6.0e-14
N 19,405
Major Consortium StudyLarge GWAS
multi-ancestry

testosterone measurement

Allele C
OR 0.04
p 2.0e-19
N 394,642
Large GWAS
European
Allele C
OR 0.04
p 8.0e-13
N 382,988
Large GWAS
European
Allele C
OR 0.45
p 1.0e-19
N 148,248
Major Consortium StudyLarge GWAS
European
Allele C
OR 0.10
p 2.0e-26
N 137,984
Major Consortium StudyLarge GWAS
multi-ancestry

About NR2F6

Enables DNA-binding transcription factor activity and sequence-specific double-stranded DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]

View all NR2F6 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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