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rs11645366

From SNPedia

Orientationplus
Stabilizedplus
Make rs11645366(C;C)
Make rs11645366(C;T)
Make rs11645366(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position62343249
is asnp
is mentioned by
dbSNPrs11645366
ebirs11645366
HLIrs11645366
Exacrs11645366
Varsomers11645366
Maprs11645366
PheGenIrs11645366
hapmaprs11645366
1000 genomesrs11645366
hgdprs11645366
ensemblrs11645366
gopubmedrs11645366
geneviewrs11645366
scholarrs11645366
googlers11645366
pharmgkbrs11645366
gwascentralrs11645366
openSNPrs11645366
23andMers11645366
23andMe allrs11645366
SNP Nexus

SNPshotrs11645366
SNPdbers11645366
MSV3drs11645366
GWAS Ctlgrs11645366
GMAF0.1322
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 0.000007
Odds Ratio None None