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rs2540917

From SNPedia

Orientationminus
Stabilizedminus
Make rs2540917(A;A)
Make rs2540917(A;G)
Make rs2540917(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position60381624
is asnp
is mentioned by
dbSNPrs2540917
ebirs2540917
HLIrs2540917
Exacrs2540917
Varsomers2540917
Maprs2540917
PheGenIrs2540917
hapmaprs2540917
1000 genomesrs2540917
hgdprs2540917
ensemblrs2540917
gopubmedrs2540917
geneviewrs2540917
scholarrs2540917
googlers2540917
pharmgkbrs2540917
gwascentralrs2540917
openSNPrs2540917
23andMers2540917
23andMe allrs2540917
SNP Nexus

SNPshotrs2540917
SNPdbers2540917
MSV3drs2540917
GWAS Ctlgrs2540917
GMAF0.2025
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 C
P-val 1E-14
Odds Ratio 0 [0.002-0.004] fl decrease


GET Evidence
rs2540917
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.1875
summary