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rs17616316

From SNPedia

Orientationplus
Stabilizedplus
Make rs17616316(C;C)
Make rs17616316(C;G)
Make rs17616316(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position103356425
is asnp
is mentioned by
dbSNPrs17616316
ebirs17616316
HLIrs17616316
Exacrs17616316
Varsomers17616316
Maprs17616316
PheGenIrs17616316
hapmaprs17616316
1000 genomesrs17616316
hgdprs17616316
ensemblrs17616316
gopubmedrs17616316
geneviewrs17616316
scholarrs17616316
googlers17616316
pharmgkbrs17616316
gwascentralrs17616316
openSNPrs17616316
23andMers17616316
23andMe allrs17616316
SNP Nexus

SNPshotrs17616316
SNPdbers17616316
MSV3drs17616316
GWAS Ctlgrs17616316
GMAF0.07805
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 G
P-val 8E-11
Odds Ratio .01 [-0.00364-0.03164] unit increase