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rs12219080

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs12219080(C;T)
Make rs12219080(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position79949523
GeneSFTPD
is asnp
is mentioned by
dbSNPrs12219080
ebirs12219080
HLIrs12219080
Exacrs12219080
Varsomers12219080
Maprs12219080
PheGenIrs12219080
hapmaprs12219080
1000 genomesrs12219080
hgdprs12219080
ensemblrs12219080
gopubmedrs12219080
geneviewrs12219080
scholarrs12219080
googlers12219080
pharmgkbrs12219080
gwascentralrs12219080
openSNPrs12219080
23andMers12219080
23andMe allrs12219080
SNP Nexus

SNPshotrs12219080
SNPdbers12219080
MSV3drs12219080
GWAS Ctlgrs12219080
GMAF0.1644
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 21858107OA-icon.png] Identifying host genetic risk factors in the context of public health surveillance for invasive pneumococcal disease