rs138190086
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs138190086(A;A) |
| Make rs138190086(A;G) |
| Make rs138190086(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 63460787 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs138190086 |
| dbSNP (classic) | rs138190086 |
| ClinGen | rs138190086 |
| ebi | rs138190086 |
| HLI | rs138190086 |
| Exac | rs138190086 |
| Gnomad | rs138190086 |
| Varsome | rs138190086 |
| LitVar | rs138190086 |
| Map | rs138190086 |
| PheGenI | rs138190086 |
| Biobank | rs138190086 |
| 1000 genomes | rs138190086 |
| hgdp | rs138190086 |
| ensembl | rs138190086 |
| geneview | rs138190086 |
| scholar | rs138190086 |
| rs138190086 | |
| pharmgkb | rs138190086 |
| gwascentral | rs138190086 |
| openSNP | rs138190086 |
| 23andMe | rs138190086 |
| SNPshot | rs138190086 |
| SNPdbe | rs138190086 |
| MSV3d | rs138190086 |
| GWAS Ctlg | rs138190086 |
| Max Magnitude | 0 |
The SNP at chr 17:61538148 was noted in the International Alzheimer Genomics Project (IGAP)
as a suggestive risk variant A/G (risk allele G) for AD with MAF=0.011 and OR=1.34 (1.20-1.50). http://www.ncbi.nlm.nih.gov/pubmed/24162737?dopt=Abstract
No rs designation was given in the article. No SNP is yet assigned to chr 17:61538148. However, a 1,922,639 base pair shift occurred from build 37 and 38 of the human genome in this region. The SNP at 17:63460787 (which corresponds to build 37) is rs138190086 A/G with MAF=0.011.
