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rs9859260

From SNPedia

Orientationplus
Stabilizedplus
Make rs9859260(C;C)
Make rs9859260(C;T)
Make rs9859260(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position196073676
GeneTFRC
is asnp
is mentioned by
dbSNPrs9859260
ebirs9859260
HLIrs9859260
Exacrs9859260
Varsomers9859260
Maprs9859260
PheGenIrs9859260
hapmaprs9859260
1000 genomesrs9859260
hgdprs9859260
ensemblrs9859260
gopubmedrs9859260
geneviewrs9859260
scholarrs9859260
googlers9859260
pharmgkbrs9859260
gwascentralrs9859260
openSNPrs9859260
23andMers9859260
23andMe allrs9859260
SNP Nexus

SNPshotrs9859260
SNPdbers9859260
MSV3drs9859260
GWAS Ctlgrs9859260
GMAF0.3701
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19862010OA-icon.png]
Trait Mean corpuscular volume
Title Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele C
P-val 8E-14
Odds Ratio 0 [0.002-0.004] fl increase


GET Evidence
rs9859260
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.445312
summary