{{Rsnum
|rsid=138190086
|Chromosome=17
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|position=63460787
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}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.