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rs7786877

From SNPedia

Orientationplus
Stabilizedplus
Make rs7786877(A;A)
Make rs7786877(A;G)
Make rs7786877(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position100616392
GeneMOSPD3
is asnp
is mentioned by
dbSNPrs7786877
ebirs7786877
HLIrs7786877
Exacrs7786877
Varsomers7786877
Maprs7786877
PheGenIrs7786877
hapmaprs7786877
1000 genomesrs7786877
hgdprs7786877
ensemblrs7786877
gopubmedrs7786877
geneviewrs7786877
scholarrs7786877
googlers7786877
pharmgkbrs7786877
gwascentralrs7786877
openSNPrs7786877
23andMers7786877
23andMe allrs7786877
SNP Nexus

SNPshotrs7786877
SNPdbers7786877
MSV3drs7786877
GWAS Ctlgrs7786877
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 G
P-val 3E-11
Odds Ratio 0 [0.002-0.004] fl increase


GET Evidence
rs7786877
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.242188
summary