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rs9276606

From SNPedia

Orientationplus
Stabilizedplus
Make rs9276606(A;A)
Make rs9276606(A;T)
Make rs9276606(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32768918
is asnp
is mentioned by
dbSNPrs9276606
ebirs9276606
HLIrs9276606
Exacrs9276606
Varsomers9276606
Maprs9276606
PheGenIrs9276606
hapmaprs9276606
1000 genomesrs9276606
hgdprs9276606
ensemblrs9276606
gopubmedrs9276606
geneviewrs9276606
scholarrs9276606
googlers9276606
pharmgkbrs9276606
gwascentralrs9276606
openSNPrs9276606
23andMers9276606
23andMe allrs9276606
SNP Nexus

SNPshotrs9276606
SNPdbers9276606
MSV3drs9276606
GWAS Ctlgrs9276606
GMAF0.2039
Max Magnitude
GWAS snp
PMID [PMID 23028341OA-icon.png]
Trait Complement C3 and C4 levels
Title Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects.
Risk Allele T
P-val 3E-22
Odds Ratio .09 [0.070-0.110] g/L decrease