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rs9373124

From SNPedia

Orientationplus
Stabilizedplus
Make rs9373124(C;C)
Make rs9373124(C;T)
Make rs9373124(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position135102071
is asnp
is mentioned by
dbSNPrs9373124
ebirs9373124
HLIrs9373124
Exacrs9373124
Varsomers9373124
Maprs9373124
PheGenIrs9373124
hapmaprs9373124
1000 genomesrs9373124
hgdprs9373124
ensemblrs9373124
gopubmedrs9373124
geneviewrs9373124
scholarrs9373124
googlers9373124
pharmgkbrs9373124
gwascentralrs9373124
openSNPrs9373124
23andMers9373124
23andMe allrs9373124
SNP Nexus

SNPshotrs9373124
SNPdbers9373124
MSV3drs9373124
GWAS Ctlgrs9373124
GMAF0.3356
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19862010OA-icon.png]
Trait Other erythrocyte phenotypes
Title Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele C
P-val 7E-14
Odds Ratio 0 [0.002-0.003] g/dl decrease
GWAS snp
PMID [PMID 21738478OA-icon.png]
Trait
Title Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population.
Risk Allele T
P-val 1E-10
Odds Ratio 0.0800 [0.06-0.10] unit increase
GET Evidence
rs9373124
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.390625
summary