rs2798224, MSANTD1

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Age at menarche
CUI: C1314691
Disease: Age at menarche
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
0.700 GeneticVariation GWASDB Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. 22387017 2012