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rs2298814

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2298814(C;T)
Make rs2298814(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position121554173
GeneSORL1
is asnp
is mentioned by
dbSNPrs2298814
ebirs2298814
HLIrs2298814
Exacrs2298814
Varsomers2298814
Maprs2298814
PheGenIrs2298814
hapmaprs2298814
1000 genomesrs2298814
hgdprs2298814
ensemblrs2298814
gopubmedrs2298814
geneviewrs2298814
scholarrs2298814
googlers2298814
pharmgkbrs2298814
gwascentralrs2298814
openSNPrs2298814
23andMers2298814
23andMe allrs2298814
SNP Nexus

SNPshotrs2298814
SNPdbers2298814
MSV3drs2298814
GWAS Ctlgrs2298814
GMAF0.04775
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs2298814
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0703125
summary