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

rs11109504

From SNPedia

Orientationplus
Stabilizedplus
Make rs11109504(A;A)
Make rs11109504(A;G)
Make rs11109504(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position78362131
is asnp
is mentioned by
dbSNPrs11109504
ebirs11109504
HLIrs11109504
Exacrs11109504
Varsomers11109504
Maprs11109504
PheGenIrs11109504
hapmaprs11109504
1000 genomesrs11109504
hgdprs11109504
ensemblrs11109504
gopubmedrs11109504
geneviewrs11109504
scholarrs11109504
googlers11109504
pharmgkbrs11109504
gwascentralrs11109504
openSNPrs11109504
23andMers11109504
23andMe allrs11109504
SNP Nexus

SNPshotrs11109504
SNPdbers11109504
MSV3drs11109504
GWAS Ctlgrs11109504
GMAF0.3379
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs11109504
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.269841
summary