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rs138190086

From SNPedia

Orientationplus
Stabilizedplus
Make rs138190086(A;A)
Make rs138190086(A;G)
Make rs138190086(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position63460787
is asnp
is mentioned by
dbSNPrs138190086
dbSNP (old)rs138190086
ClinGenrs138190086
ebirs138190086
HLIrs138190086
Exacrs138190086
Gnomadrs138190086
Varsomers138190086
Maprs138190086
PheGenIrs138190086
Biobankrs138190086
1000 genomesrs138190086
hgdprs138190086
ensemblrs138190086
gopubmedrs138190086
geneviewrs138190086
scholarrs138190086
googlers138190086
pharmgkbrs138190086
gwascentralrs138190086
openSNPrs138190086
23andMers138190086
23andMe allrs138190086
SNP Nexus

SNPshotrs138190086
SNPdbers138190086
MSV3drs138190086
GWAS Ctlgrs138190086
Max Magnitude
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.