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rs7775698

From SNPedia

Orientationplus
Stabilizedplus
Make rs7775698(C;C)
Make rs7775698(C;T)
Make rs7775698(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position135097497
is asnp
is mentioned by
dbSNPrs7775698
ebirs7775698
HLIrs7775698
Exacrs7775698
Varsomers7775698
Maprs7775698
PheGenIrs7775698
hapmaprs7775698
1000 genomesrs7775698
hgdprs7775698
ensemblrs7775698
gopubmedrs7775698
geneviewrs7775698
scholarrs7775698
googlers7775698
pharmgkbrs7775698
gwascentralrs7775698
openSNPrs7775698
23andMers7775698
23andMe allrs7775698
SNP Nexus

SNPshotrs7775698
SNPdbers7775698
MSV3drs7775698
GWAS Ctlgrs7775698
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20139978]
Trait Hematological and biochemical traits
Title Genome-wide association study of hematological and biochemical traits in a Japanese population
Risk Allele T
P-val 3E-66
Odds Ratio 2.01 [NR] % variance
GWAS snp
PMID [PMID 19853236OA-icon.png]
Trait Hematology traits
Title Sequence variants in three loci influence monocyte counts and erythrocyte volume
Risk Allele C
P-val 5E-13
Odds Ratio 0.19 [0.13-0.25] s.d. decrease
GWAS snp
PMID [PMID 20927387OA-icon.png]
Trait
Title A genome-wide association study of red blood cell traits using the electronic medical record
Risk Allele T
P-val 1E-14
Odds Ratio 0.09 [0.07-0.11] unit decrease
GWAS snp
PMID [PMID 23263863OA-icon.png]
Trait Mean corpuscular volume
Title GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.
Risk Allele T
P-val 2E-9
Odds Ratio .54 [0.37-0.72] unit increase