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rs3800569

From SNPedia

Orientationminus
Stabilizedminus
Make rs3800569(A;A)
Make rs3800569(A;G)
Make rs3800569(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position138726680
GeneATP6V0A4
is asnp
is mentioned by
dbSNPrs3800569
ebirs3800569
HLIrs3800569
Exacrs3800569
Varsomers3800569
Maprs3800569
PheGenIrs3800569
hapmaprs3800569
1000 genomesrs3800569
hgdprs3800569
ensemblrs3800569
gopubmedrs3800569
geneviewrs3800569
scholarrs3800569
googlers3800569
pharmgkbrs3800569
gwascentralrs3800569
openSNPrs3800569
23andMers3800569
23andMe allrs3800569
SNP Nexus

SNPshotrs3800569
SNPdbers3800569
MSV3drs3800569
GWAS Ctlgrs3800569
GMAF0.2094
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21326311]
Trait
Title Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients
Risk Allele C
P-val 0.000006
Odds Ratio 1.2000 [0.69-1.71] unit increase