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rs10487372

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10487372(C;T)
Make rs10487372(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117560845
GeneCFTR
is asnp
is mentioned by
dbSNPrs10487372
ebirs10487372
HLIrs10487372
Exacrs10487372
Varsomers10487372
Maprs10487372
PheGenIrs10487372
hapmaprs10487372
1000 genomesrs10487372
hgdprs10487372
ensemblrs10487372
gopubmedrs10487372
geneviewrs10487372
scholarrs10487372
googlers10487372
pharmgkbrs10487372
gwascentralrs10487372
openSNPrs10487372
23andMers10487372
23andMe allrs10487372
SNP Nexus

SNPshotrs10487372
SNPdbers10487372
MSV3drs10487372
GWAS Ctlgrs10487372
GMAF0.1079
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 20116881OA-icon.png] Cystic fibrosis transmembrane conductance regulator gene mutation and lung cancer risk