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rs12793173

From SNPedia

Orientationplus
Stabilizedplus
Make rs12793173(C;C)
Make rs12793173(C;T)
Make rs12793173(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position34812657
is asnp
is mentioned by
dbSNPrs12793173
ebirs12793173
HLIrs12793173
Exacrs12793173
Varsomers12793173
Maprs12793173
PheGenIrs12793173
hapmaprs12793173
1000 genomesrs12793173
hgdprs12793173
ensemblrs12793173
gopubmedrs12793173
geneviewrs12793173
scholarrs12793173
googlers12793173
pharmgkbrs12793173
gwascentralrs12793173
openSNPrs12793173
23andMers12793173
23andMe allrs12793173
SNP Nexus

SNPshotrs12793173
SNPdbers12793173
MSV3drs12793173
GWAS Ctlgrs12793173
GMAF0.163
Max Magnitude
? (C;C) (C;T) (T;T) 28
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-9
Odds Ratio None None