Variant: rs3779381

present in Gene: WNT16 present in Chromosome: 7 Position on Chromosome: 121326736 Alleles of this Variant: A/G

rs3779381 in WNT16 gene and Bone Mineral Density Test PMID 22792070 2012 Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus.

rs3779381 in WNT16 gene and Ischemic cardiomyopathy PMID 30251476 2019 Identification of a 3'-Untranslated Genetic Variant of RARB Associated With Carotid Intima-Media Thickness in Rheumatoid Arthritis: A Genome-Wide Association Study.

rs3779381 in WNT16 gene and Rheumatoid Arthritis PMID 30251476 2019 Identification of a 3'-Untranslated Genetic Variant of RARB Associated With Carotid Intima-Media Thickness in Rheumatoid Arthritis: A Genome-Wide Association Study.