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rs9985399

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs9985399(C;C)
Make rs9985399(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position39967143
GeneMYRIP
is asnp
is mentioned by
dbSNPrs9985399
ClinGenrs9985399
ebirs9985399
HLIrs9985399
Exacrs9985399
Varsomers9985399
Maprs9985399
PheGenIrs9985399
hapmaprs9985399
1000 genomesrs9985399
hgdprs9985399
ensemblrs9985399
gopubmedrs9985399
geneviewrs9985399
scholarrs9985399
googlers9985399
pharmgkbrs9985399
gwascentralrs9985399
openSNPrs9985399
23andMers9985399
23andMe allrs9985399
SNP Nexus

SNPshotrs9985399
SNPdbers9985399
MSV3drs9985399
GWAS Ctlgrs9985399
GMAF0.2259
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21130836OA-icon.png]
Trait
Title Whole genome association scan for genetic polymorphisms influencing information processing speed
Risk Allele T
P-val 0.000009
Odds Ratio 0.2600 [0.14-0.38] unit decrease