Have questions? Visit https://www.reddit.com/r/SNPedia

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
ebirs9349205
HLIrs9349205
Exacrs9349205
Varsomers9349205
Maprs9349205
PheGenIrs9349205
hapmaprs9349205
1000 genomesrs9349205
hgdprs9349205
ensemblrs9349205
gopubmedrs9349205
geneviewrs9349205
scholarrs9349205
googlers9349205
pharmgkbrs9349205
gwascentralrs9349205
openSNPrs9349205
23andMers9349205
23andMe allrs9349205
SNP Nexus

SNPshotrs9349205
SNPdbers9349205
MSV3drs9349205
GWAS Ctlgrs9349205
GMAF0.1731
Max Magnitude
? (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


GET Evidence
rs9349205
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.164062
summary