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From SNPedia

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.