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rs7255045

From SNPedia

Orientationplus
Stabilizedplus
Make rs7255045(A;A)
Make rs7255045(A;G)
Make rs7255045(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position12821455
is asnp
is mentioned by
dbSNPrs7255045
ebirs7255045
HLIrs7255045
Exacrs7255045
Varsomers7255045
Maprs7255045
PheGenIrs7255045
hapmaprs7255045
1000 genomesrs7255045
hgdprs7255045
ensemblrs7255045
gopubmedrs7255045
geneviewrs7255045
scholarrs7255045
googlers7255045
pharmgkbrs7255045
gwascentralrs7255045
openSNPrs7255045
23andMers7255045
23andMe allrs7255045
SNP Nexus

SNPshotrs7255045
SNPdbers7255045
MSV3drs7255045
GWAS Ctlgrs7255045
GMAF0.4132
Max Magnitude
? (A;A) (A;G) (G;G) 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 2E-12
Odds Ratio 0 [0.002-0.004] fl decrease
GET Evidence
rs7255045
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.484375
summary