Have questions? Visit https://www.reddit.com/r/SNPedia

rs1784919

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1784919(A;A)
Make rs1784919(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position121568956
GeneSORL1
is asnp
is mentioned by
dbSNPrs1784919
ebirs1784919
HLIrs1784919
Exacrs1784919
Varsomers1784919
Maprs1784919
PheGenIrs1784919
hapmaprs1784919
1000 genomesrs1784919
hgdprs1784919
ensemblrs1784919
gopubmedrs1784919
geneviewrs1784919
scholarrs1784919
googlers1784919
pharmgkbrs1784919
gwascentralrs1784919
openSNPrs1784919
23andMers1784919
23andMe allrs1784919
SNP Nexus

SNPshotrs1784919
SNPdbers1784919
MSV3drs1784919
GWAS Ctlgrs1784919
GMAF0.06107
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GET Evidence
rs1784919
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.858333
summary