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rs7189020

From SNPedia

Orientationplus
Stabilizedplus
Make rs7189020(A;A)
Make rs7189020(A;T)
Make rs7189020(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position254804
GeneITFG3
is asnp
is mentioned by
dbSNPrs7189020
ebirs7189020
HLIrs7189020
Exacrs7189020
Varsomers7189020
Maprs7189020
PheGenIrs7189020
hapmaprs7189020
1000 genomesrs7189020
hgdprs7189020
ensemblrs7189020
gopubmedrs7189020
geneviewrs7189020
scholarrs7189020
googlers7189020
pharmgkbrs7189020
gwascentralrs7189020
openSNPrs7189020
23andMers7189020
23andMe allrs7189020
SNP Nexus

SNPshotrs7189020
SNPdbers7189020
MSV3drs7189020
GWAS Ctlgrs7189020
GMAF0.405
Max Magnitude
? (A;A) (A;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 T
P-val 2E-12
Odds Ratio 0 [0.002-0.004] fl decrease
GET Evidence
rs7189020
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.648438
summary