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rs12351590

From SNPedia

Orientationplus
Stabilizedplus
Make rs12351590(A;A)
Make rs12351590(A;G)
Make rs12351590(G;G)
ReferenceGRCh37.p10 37.5/138
Chromosome9
Position12108916
is asnp
is mentioned by
dbSNPrs12351590
ebirs12351590
HLIrs12351590
Exacrs12351590
Varsomers12351590
Maprs12351590
PheGenIrs12351590
hapmaprs12351590
1000 genomesrs12351590
hgdprs12351590
ensemblrs12351590
gopubmedrs12351590
geneviewrs12351590
scholarrs12351590
googlers12351590
pharmgkbrs12351590
gwascentralrs12351590
openSNPrs12351590
23andMers12351590
23andMe allrs12351590
SNP Nexus

SNPshotrs12351590
SNPdbers12351590
MSV3drs12351590
GWAS Ctlgrs12351590
GMAF0.2475
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23738518OA-icon.png]
Trait Reading and spelling
Title A genome-wide association study for reading and language abilities in two population cohorts.
Risk Allele
P-val 3E-6
Odds Ratio NR NR


[PMID 20525348OA-icon.png] Copy number variation and cytidine analogue cytotoxicity: a genome-wide association approach.