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rs1329060

From SNPedia

Orientationminus
Stabilizedminus
Make rs1329060(A;A)
Make rs1329060(A;G)
Make rs1329060(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position117676199
is asnp
is mentioned by
dbSNPrs1329060
dbSNP (classic)rs1329060
ClinGenrs1329060
ebirs1329060
HLIrs1329060
Exacrs1329060
Gnomadrs1329060
Varsomers1329060
LitVarrs1329060
Maprs1329060
PheGenIrs1329060
Biobankrs1329060
1000 genomesrs1329060
hgdprs1329060
ensemblrs1329060
geneviewrs1329060
scholarrs1329060
googlers1329060
pharmgkbrs1329060
gwascentralrs1329060
openSNPrs1329060
23andMers1329060
SNPshotrs1329060
SNPdbers1329060
MSV3drs1329060
GWAS Ctlgrs1329060
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 26177520OA-icon.png] Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus