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rs17110690

From SNPedia

Orientationplus
Stabilizedplus
Make rs17110690(A;A)
Make rs17110690(A;G)
Make rs17110690(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position72014217
GeneTPH2
is asnp
is mentioned by
dbSNPrs17110690
ebirs17110690
HLIrs17110690
Exacrs17110690
Varsomers17110690
Maprs17110690
PheGenIrs17110690
hapmaprs17110690
1000 genomesrs17110690
hgdprs17110690
ensemblrs17110690
gopubmedrs17110690
geneviewrs17110690
scholarrs17110690
googlers17110690
pharmgkbrs17110690
gwascentralrs17110690
openSNPrs17110690
23andMers17110690
23andMe allrs17110690
SNP Nexus

SNPshotrs17110690
SNPdbers17110690
MSV3drs17110690
GWAS Ctlgrs17110690
GMAF0.2172
Max Magnitude
? (A;A) (A;G) (G;G) 28



GET Evidence
rs17110690
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0952381
summary



[PMID 25875332OA-icon.png] Genome-Wide Analysis of Attention Deficit Hyperactivity Disorder in Norway