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rs17135859

From SNPedia

Orientationplus
Stabilizedplus
Make rs17135859(C;C)
Make rs17135859(C;T)
Make rs17135859(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position113660957
is asnp
is mentioned by
dbSNPrs17135859
ebirs17135859
HLIrs17135859
Exacrs17135859
Varsomers17135859
Maprs17135859
PheGenIrs17135859
hapmaprs17135859
1000 genomesrs17135859
hgdprs17135859
ensemblrs17135859
gopubmedrs17135859
geneviewrs17135859
scholarrs17135859
googlers17135859
pharmgkbrs17135859
gwascentralrs17135859
openSNPrs17135859
23andMers17135859
23andMe allrs17135859
SNP Nexus

SNPshotrs17135859
SNPdbers17135859
MSV3drs17135859
GWAS Ctlgrs17135859
GMAF0.1322
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21326311]
Trait
Title Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients
Risk Allele C
P-val 0.000008
Odds Ratio 0.9700 [0.54-1.40] unit increase