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rs9494145

From SNPedia

Orientationplus
Stabilizedplus
Make rs9494145(C;C)
Make rs9494145(C;T)
Make rs9494145(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position135111414
is asnp
is mentioned by
dbSNPrs9494145
ebirs9494145
HLIrs9494145
Exacrs9494145
Varsomers9494145
Maprs9494145
PheGenIrs9494145
hapmaprs9494145
1000 genomesrs9494145
hgdprs9494145
ensemblrs9494145
gopubmedrs9494145
geneviewrs9494145
scholarrs9494145
googlers9494145
pharmgkbrs9494145
gwascentralrs9494145
openSNPrs9494145
23andMers9494145
23andMe allrs9494145
SNP Nexus

SNPshotrs9494145
SNPdbers9494145
MSV3drs9494145
GWAS Ctlgrs9494145
GMAF0.1905
Max Magnitude
? (C;C) (C;T) (T;T) 28
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 C
P-val 3E-15
Odds Ratio 0.98 [0.74-1.22] unit increase
GWAS snp
PMID [PMID 22423221OA-icon.png]
Trait
Title A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans.
Risk Allele T
P-val 3E-9
Odds Ratio 8.1900 None


[PMID 19860791] Genetic evidence for a role of IL33 in nasal polyposis.


GET Evidence
rs9494145
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.179688
summary



Persistant Fetal Hemoglobin


[PMID 25928412OA-icon.png] Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer