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rs9349205

From SNPedia

Orientationplus
Stabilizedplus
Make rs9349205(A;A)
Make rs9349205(A;G)
Make rs9349205(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position41957421
GeneCCND3
is asnp
is mentioned by
dbSNPrs9349205
dbSNP (classic)rs9349205
ClinGenrs9349205
ebirs9349205
HLIrs9349205
Exacrs9349205
Gnomadrs9349205
Varsomers9349205
LitVarrs9349205
Maprs9349205
PheGenIrs9349205
Biobankrs9349205
1000 genomesrs9349205
hgdprs9349205
ensemblrs9349205
geneviewrs9349205
scholarrs9349205
googlers9349205
pharmgkbrs9349205
gwascentralrs9349205
openSNPrs9349205
23andMers9349205
SNPshotrs9349205
SNPdbers9349205
MSV3drs9349205
GWAS Ctlgrs9349205
GMAF0.1731
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 19862010OA-icon.png]
Trait Mean corpuscular hemoglobin
Title Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele A
P-val 8E-20
Odds Ratio 0.01 [0.004-0.006] pg decrease