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rs11201887

From SNPedia

Orientationplus
Stabilizedplus
Make rs11201887(C;C)
Make rs11201887(C;T)
Make rs11201887(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position86124353
GeneGRID1
is asnp
is mentioned by
dbSNPrs11201887
ebirs11201887
HLIrs11201887
Exacrs11201887
Varsomers11201887
Maprs11201887
PheGenIrs11201887
hapmaprs11201887
1000 genomesrs11201887
hgdprs11201887
ensemblrs11201887
gopubmedrs11201887
geneviewrs11201887
scholarrs11201887
googlers11201887
pharmgkbrs11201887
gwascentralrs11201887
openSNPrs11201887
23andMers11201887
23andMe allrs11201887
SNP Nexus

SNPshotrs11201887
SNPdbers11201887
MSV3drs11201887
GWAS Ctlgrs11201887
GMAF0.4417
Max Magnitude
? (C;C) (C;T) (T;T) 28
GET Evidence
rs11201887
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.539062
summary