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rs12718597

From SNPedia

Orientationplus
Stabilizedplus
Make rs12718597(A;A)
Make rs12718597(A;C)
Make rs12718597(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position50360730
GeneIKZF1, LOC102723522
is asnp
is mentioned by
dbSNPrs12718597
ebirs12718597
HLIrs12718597
Exacrs12718597
Varsomers12718597
Maprs12718597
PheGenIrs12718597
hapmaprs12718597
1000 genomesrs12718597
hgdprs12718597
ensemblrs12718597
gopubmedrs12718597
geneviewrs12718597
scholarrs12718597
googlers12718597
pharmgkbrs12718597
gwascentralrs12718597
openSNPrs12718597
23andMers12718597
23andMe allrs12718597
SNP Nexus

SNPshotrs12718597
SNPdbers12718597
MSV3drs12718597
GWAS Ctlgrs12718597
GMAF0.298
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 19862010OA-icon.png]
Trait Mean corpuscular volume
Title Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele A
P-val 5E-13
Odds Ratio 0 [0.002-0.004] fl increase


GET Evidence
rs12718597
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.245902
summary