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rs7610017

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs7610017(A;A)
Make rs7610017(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position189625635
is asnp
is mentioned by
dbSNPrs7610017
ebirs7610017
HLIrs7610017
Exacrs7610017
Varsomers7610017
Maprs7610017
PheGenIrs7610017
hapmaprs7610017
1000 genomesrs7610017
hgdprs7610017
ensemblrs7610017
gopubmedrs7610017
geneviewrs7610017
scholarrs7610017
googlers7610017
pharmgkbrs7610017
gwascentralrs7610017
openSNPrs7610017
23andMers7610017
23andMe allrs7610017
SNP Nexus

SNPshotrs7610017
SNPdbers7610017
MSV3drs7610017
GWAS Ctlgrs7610017
GMAF0.09642
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20100581OA-icon.png]
Trait Brain imaging
Title Whole Genome Association Study of Brain-Wide Imaging Phenotypes for Identifying Quantitative Trait Loci in MCI and AD: A Study of the ADNI Cohort
Risk Allele
P-val NS
Odds Ratio None None