From: Genotype-expression interactions for BDNF across human brain regions
SNP rsID | 1000 Genome Frequency | Location | Associated Disorder or Phenotype |
---|---|---|---|
rs16917204 | C = 0.2298 | Intron, gene body, Chromosome 11, Position: 27646808 | • Methamphetamine abuse [15] |
• Panic disorders [16] | |||
• Alzheimers Disease [17] | |||
• Schizophrenia [18] | |||
rs6265 | T = 0.2013 | Exon, gene body, Chromosome 11, Position: 27658369 | • Major depressive disorder [19] |
• Bipolar disorder [20] | |||
• Obsessive-compulsive disorder [21] | |||
• Alzheimer’s disease [22] | |||
rs11030104 | G = 0.2226 | Intron, gene body, Chromosome 11, Position: 27662970 | • Increased BMI [23] |
• BMI and Smoking [24] | |||
• Alzheimer’s disease [22] | |||
rs7103411 | C = 0.2470 | Intron, gene body, Chromosome 11, Position: 27678578 | • Epilepsy [25] |
rs16917237 | T = 0.2214 | Intron, gene body, Chromosome 11, Position: 27680836 | • Eating disorders, increased BMI [26] |
• Bipolar disorder [27] | |||
rs6484320 | T = 0.2468 | Intron, gene body, Chromosome 11, Position: 27681641 | • Epilepsy (in Fragile x-syndrome) [28] |
• Smoking and nicotine addiction [29] | |||
rs988748 | C = 0.2430 | Intron, gene body, Chromosome 11, Position: 27703198 | • Major depressive disorder [19] |
• Smoking and nicotine addiction [29] | |||
rs2049045 | C = 0.0629 | Intron, gene body, Chromosome 11, Position: 27672694 | • Alzheimer’s disease-related depression [30] |
• Bipolar disorder [31] | |||
• Alzheimer’s disease [22] |