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rs2180566

From SNPedia

Orientationplus
Stabilizedplus
Make rs2180566(C;C)
Make rs2180566(C;T)
Make rs2180566(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position31431051
GeneDEFB122
is asnp
is mentioned by
dbSNPrs2180566
ebirs2180566
HLIrs2180566
Exacrs2180566
Varsomers2180566
Maprs2180566
PheGenIrs2180566
hapmaprs2180566
1000 genomesrs2180566
hgdprs2180566
ensemblrs2180566
gopubmedrs2180566
geneviewrs2180566
scholarrs2180566
googlers2180566
pharmgkbrs2180566
gwascentralrs2180566
openSNPrs2180566
23andMers2180566
23andMe allrs2180566
SNP Nexus

SNPshotrs2180566
SNPdbers2180566
MSV3drs2180566
GWAS Ctlgrs2180566
GMAF0.4146
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs2180566
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.585938
summary