rs314277
This variant is located in the LIN28B gene.
▶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.
age at menarche
BMI-adjusted hip circumference
BMI-adjusted waist circumference
body height
digit length ratio
▶Research that mentions this SNP (3)
▶Associations of polymorphisms in the genes of FGFR2, FGF1, and RBFOX2 with breast cancer risk by estrogen/progesterone receptor statusAssociationN=2,416Yu‐Ling Cen et al.(2013)· Molecular Carcinogenesis
A hospital-based case-control study in rural and urban India (1,204 cases; 1,212 controls) examined genetic and lifestyle risk factors for breast cancer. Four SNPs in FGFR2 (rs1219648, rs2420946, rs2981575, rs2981582) showed positive associations with breast cancer (ORs 1.32-1.47). Additional SNPs in obesity and metabolic genes (rs374748 in FBN2, rs2922763 in HNF4G, rs2116830 in KCNMA1, rs11121832 in MTHFR, rs16886165 in MAP3K1, rs11594610 in TCF7L2, rs2274459 in MLN) were associated with increased breast cancer risk. Waist-to-hip ratio ≥0.95 showed strong association (OR 3.78; 95% CI 2.92-4.89), and women living first 20 years in rural areas showed protective effect (OR 0.77).
▶Genetic association suggests that SMOC1 mediates between prenatal sex hormones and digit ratioAssociationN=979Lawrance-Owen AJ et al.(2013)· Human Genetics
A genome-wide association study of 979 healthy adults identified SMOC1 as a novel locus strongly associated with digit ratio (2D:4D), a biomarker of prenatal sex hormone exposure. The strongest association was at rs4902759 (P = 1.41 × 10⁻⁸), with each additional C allele decreasing 2D:4D by 0.0076. Meta-analysis with an independent study yielded P = 1.5 × 10⁻¹¹. The authors propose that SMOC1, a gene critical for limb development that is regulated by sex hormones, mediates the relationship between prenatal hormone exposure and digit ratio.
▶Genome-wide association scan for stature in Chinese: evidence for ethnic specific lociAssociationN=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.
About LIN28B
The protein encoded by this gene belongs to the lin-28 family, which is characterized by the presence of a cold-shock domain and a pair of CCHC zinc finger domains. This gene is highly expressed in testis, fetal liver, placenta, and in primary human tumors and cancer cell lines. It is negatively regulated by microRNAs that target sites in the 3' UTR, and overexpression of this gene in primary tumors is linked to the repression of let-7 family of microRNAs and derepression of let-7 targets, which facilitates cellular transformation. [provided by RefSeq, Jun 2012]
View all LIN28B variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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