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rs2270447

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2270447(C;C)
Make rs2270447(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position162103238
is asnp
is mentioned by
dbSNPrs2270447
ebirs2270447
HLIrs2270447
Exacrs2270447
Varsomers2270447
Maprs2270447
PheGenIrs2270447
hapmaprs2270447
1000 genomesrs2270447
hgdprs2270447
ensemblrs2270447
gopubmedrs2270447
geneviewrs2270447
scholarrs2270447
googlers2270447
pharmgkbrs2270447
gwascentralrs2270447
openSNPrs2270447
23andMers2270447
23andMe allrs2270447
SNP Nexus

SNPshotrs2270447
SNPdbers2270447
MSV3drs2270447
GWAS Ctlgrs2270447
GMAF0.18
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20585627OA-icon.png]
Trait Common traits (Other)
Title Web-based, participant-driven studies yield novel genetic associations for common traits
Risk Allele
P-val 8E-7
Odds Ratio None None