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rs17371334

From SNPedia

Orientationplus
Stabilizedplus
Make rs17371334(G;G)
Make rs17371334(G;T)
Make rs17371334(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position84458192
GeneLINC00333
is asnp
is mentioned by
dbSNPrs17371334
ebirs17371334
HLIrs17371334
Exacrs17371334
Varsomers17371334
Maprs17371334
PheGenIrs17371334
hapmaprs17371334
1000 genomesrs17371334
hgdprs17371334
ensemblrs17371334
gopubmedrs17371334
geneviewrs17371334
scholarrs17371334
googlers17371334
pharmgkbrs17371334
gwascentralrs17371334
openSNPrs17371334
23andMers17371334
23andMe allrs17371334
SNP Nexus

SNPshotrs17371334
SNPdbers17371334
MSV3drs17371334
GWAS Ctlgrs17371334
GMAF0.253
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 22365631OA-icon.png]
Trait
Title Genome-Wide Association Study of Temperament in Bipolar Disorder Reveals Significant Associations with Three Novel Loci.
Risk Allele
P-val 0.000002
Odds Ratio 1.0500 None


GET Evidence
rs17371334
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.289062
summary