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rs11717368

From SNPedia

Orientationplus
Stabilizedplus
Make rs11717368(C;C)
Make rs11717368(C;G)
Make rs11717368(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position196107486
is asnp
is mentioned by
dbSNPrs11717368
ebirs11717368
HLIrs11717368
Exacrs11717368
Varsomers11717368
Maprs11717368
PheGenIrs11717368
hapmaprs11717368
1000 genomesrs11717368
hgdprs11717368
ensemblrs11717368
gopubmedrs11717368
geneviewrs11717368
scholarrs11717368
googlers11717368
pharmgkbrs11717368
gwascentralrs11717368
openSNPrs11717368
23andMers11717368
23andMe allrs11717368
SNP Nexus

SNPshotrs11717368
SNPdbers11717368
MSV3drs11717368
GWAS Ctlgrs11717368
GMAF0.3489
Max Magnitude
? (C;C) (C;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 C
P-val 7E-19
Odds Ratio .01 [0.00016-0.01584] unit increase