rs4743034

This is a intron variant variant in the ZNF462 gene.

GWAS Catalog Trait Associations (4)

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

IGF-1 measurement

Sinnott-Armstrong N et al. Genetics of 35 blood and urine biomarkers in the UK Biobank. Nature Genetics 53(2):185-194 (2021)
Allele A
OR 0.02
p 9.0e-15
N 353,824
Major Consortium StudyLarge GWAS
multi-ancestry

atrial fibrillation

Roselli C et al. Multi-ethnic genome-wide association study for atrial fibrillation. Nature Genetics 50(9):1225-1233 (2018)
Allele A
OR 1.05
p 4.0e-9
N 588,190
Large GWAS
multi-ancestry

body height

Gudbjartsson DF et al. Many sequence variants affecting diversity of adult human height. Nature Genetics 40(5):609-15 (2008)
Allele A
OR 5.30
p 2.0e-8
N 30,968
Large GWAS
European

Research that mentions this SNP (1)

Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci
AssociationN=3,571Shu-Feng Lei et al.(2009)· Human Genetics

Genome-wide association study in 618 Northern Chinese and replication in 2,953 Southern Chinese identified 13 contiguous SNPs in the ZNF510/ZNF782 region significantly associated with stature (P = 9.71×10^-5 to 3.11×10^-6, FDR q = 0.036-0.046). The most significant SNP rs10816533 replicated in Southern Chinese (P = 0.029, combined P = 1.55×10^-6), suggesting this is an ethnic-specific locus for height variation in Chinese populations.

Traits studied:Adult heightHuman stature

About ZNF462

The protein encoded by this gene belongs to C2H2-type zinc finger family of proteins. It contains multiple C2H2-type zinc fingers and may be involved in transcriptional regulation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]

View all ZNF462 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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