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rs17852153

From SNPedia

Merged intors9344
Orientationplus
Stabilizedplus
Make rs17852153(A;A)
Make rs17852153(A;G)
Make rs17852153(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position69648142
GeneCCND1, LOC100996515
is asnp
is mentioned by
dbSNPrs17852153
ebirs17852153
HLIrs17852153
Exacrs17852153
Varsomers17852153
Maprs17852153
PheGenIrs17852153
hapmaprs17852153
1000 genomesrs17852153
hgdprs17852153
ensemblrs17852153
gopubmedrs17852153
geneviewrs17852153
scholarrs17852153
googlers17852153
pharmgkbrs17852153
gwascentralrs17852153
openSNPrs17852153
23andMers17852153
23andMe allrs17852153
SNP Nexus

SNPshotrs17852153
SNPdbers17852153
MSV3drs17852153
GWAS Ctlgrs17852153
StatusMerged into rs9344
Max Magnitude
? (A;A) (A;G) (G;G) 28
GET Evidence
rs17852153
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.335938
summary