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rs2306168

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2306168(C;T)
Make rs2306168(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position75196537
GeneSLCO2B1
is asnp
is mentioned by
dbSNPrs2306168
ebirs2306168
HLIrs2306168
Exacrs2306168
Varsomers2306168
Maprs2306168
PheGenIrs2306168
hapmaprs2306168
1000 genomesrs2306168
hgdprs2306168
ensemblrs2306168
gopubmedrs2306168
geneviewrs2306168
scholarrs2306168
googlers2306168
pharmgkbrs2306168
gwascentralrs2306168
openSNPrs2306168
23andMers2306168
23andMe allrs2306168
SNP Nexus

SNPshotrs2306168
SNPdbers2306168
MSV3drs2306168
GWAS Ctlgrs2306168
GMAF0.1763
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
SLCO2B1-S486F
aa_change Ser486Phe
aa_change_short S486F
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.130972
summary



[PMID 23666051OA-icon.png] SLCO2B1 genetic polymorphisms in a Korean population: pyrosequencing analyses and comprehensive comparison with other populations.