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rs11666638

From SNPedia

Orientationplus
Stabilizedplus
Make rs11666638(A;A)
Make rs11666638(A;G)
Make rs11666638(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position34120844
is asnp
is mentioned by
dbSNPrs11666638
ebirs11666638
HLIrs11666638
Exacrs11666638
Varsomers11666638
Maprs11666638
PheGenIrs11666638
hapmaprs11666638
1000 genomesrs11666638
hgdprs11666638
ensemblrs11666638
gopubmedrs11666638
geneviewrs11666638
scholarrs11666638
googlers11666638
pharmgkbrs11666638
gwascentralrs11666638
openSNPrs11666638
23andMers11666638
23andMe allrs11666638
SNP Nexus

SNPshotrs11666638
SNPdbers11666638
MSV3drs11666638
GWAS Ctlgrs11666638
GMAF0.2704
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs11666638
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.3125
summary