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rs11611647

From SNPedia

Orientationplus
Stabilizedplus
Make rs11611647(C;C)
Make rs11611647(C;T)
Make rs11611647(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position4224753
is asnp
is mentioned by
dbSNPrs11611647
ebirs11611647
HLIrs11611647
Exacrs11611647
Varsomers11611647
Maprs11611647
PheGenIrs11611647
hapmaprs11611647
1000 genomesrs11611647
hgdprs11611647
ensemblrs11611647
gopubmedrs11611647
geneviewrs11611647
scholarrs11611647
googlers11611647
pharmgkbrs11611647
gwascentralrs11611647
openSNPrs11611647
23andMers11611647
23andMe allrs11611647
SNP Nexus

SNPshotrs11611647
SNPdbers11611647
MSV3drs11611647
GWAS Ctlgrs11611647
GMAF0.2374
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 C
P-val 6E-9
Odds Ratio 0.23 [NR] % variance