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rs9268905

From SNPedia

Orientationplus
Stabilizedplus
Make rs9268905(C;C)
Make rs9268905(C;G)
Make rs9268905(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32464300
is asnp
is mentioned by
dbSNPrs9268905
ebirs9268905
HLIrs9268905
Exacrs9268905
Varsomers9268905
Maprs9268905
PheGenIrs9268905
hapmaprs9268905
1000 genomesrs9268905
hgdprs9268905
ensemblrs9268905
gopubmedrs9268905
geneviewrs9268905
scholarrs9268905
googlers9268905
pharmgkbrs9268905
gwascentralrs9268905
openSNPrs9268905
23andMers9268905
23andMe allrs9268905
SNP Nexus

SNPshotrs9268905
SNPdbers9268905
MSV3drs9268905
GWAS Ctlgrs9268905
GMAF0.2934
Max Magnitude
GWAS snp
PMID [PMID 21602797OA-icon.png]
Trait
Title Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.
Risk Allele C
P-val 1E-7
Odds Ratio None None