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rs11190134

From SNPedia

Orientationplus
Stabilizedplus
Make rs11190134(A;A)
Make rs11190134(A;G)
Make rs11190134(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position99522443
is asnp
is mentioned by
dbSNPrs11190134
ebirs11190134
HLIrs11190134
Exacrs11190134
Varsomers11190134
Maprs11190134
PheGenIrs11190134
hapmaprs11190134
1000 genomesrs11190134
hgdprs11190134
ensemblrs11190134
gopubmedrs11190134
geneviewrs11190134
scholarrs11190134
googlers11190134
pharmgkbrs11190134
gwascentralrs11190134
openSNPrs11190134
23andMers11190134
23andMe allrs11190134
SNP Nexus

SNPshotrs11190134
SNPdbers11190134
MSV3drs11190134
GWAS Ctlgrs11190134
GMAF0.3893
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23222517OA-icon.png]
Trait Red blood cell traits
Title Seventy-five genetic loci influencing the human red blood cell.
Risk Allele G
P-val 1E-10
Odds Ratio .01 [0.0032-0.0188] unit decrease