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rs11218342

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs11218342(C;C)
Make rs11218342(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position121563719
GeneSORL1
is asnp
is mentioned by
dbSNPrs11218342
ebirs11218342
HLIrs11218342
Exacrs11218342
Varsomers11218342
Maprs11218342
PheGenIrs11218342
hapmaprs11218342
1000 genomesrs11218342
hgdprs11218342
ensemblrs11218342
gopubmedrs11218342
geneviewrs11218342
scholarrs11218342
googlers11218342
pharmgkbrs11218342
gwascentralrs11218342
openSNPrs11218342
23andMers11218342
23andMe allrs11218342
SNP Nexus

SNPshotrs11218342
SNPdbers11218342
MSV3drs11218342
GWAS Ctlgrs11218342
GMAF0.04775
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs11218342
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0703125
summary