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rs643381

From SNPedia

Orientationplus
Stabilizedplus
Make rs643381(A;A)
Make rs643381(A;C)
Make rs643381(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position139518286
is asnp
is mentioned by
dbSNPrs643381
ClinGenrs643381
ebirs643381
HLIrs643381
Exacrs643381
Varsomers643381
Maprs643381
PheGenIrs643381
hapmaprs643381
1000 genomesrs643381
hgdprs643381
ensemblrs643381
gopubmedrs643381
geneviewrs643381
scholarrs643381
googlers643381
pharmgkbrs643381
gwascentralrs643381
openSNPrs643381
23andMers643381
23andMe allrs643381
SNP Nexus

SNPshotrs643381
SNPdbers643381
MSV3drs643381
GWAS Ctlgrs643381
GMAF0.3517
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-25
Odds Ratio 0 [0.003-0.005] fl decrease


GET Evidence
rs643381
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.354545
summary