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rs17079247

From SNPedia

Orientationplus
Stabilizedplus
Make rs17079247(C;C)
Make rs17079247(C;T)
Make rs17079247(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position85091744
is asnp
is mentioned by
dbSNPrs17079247
ebirs17079247
HLIrs17079247
Exacrs17079247
Varsomers17079247
Maprs17079247
PheGenIrs17079247
hapmaprs17079247
1000 genomesrs17079247
hgdprs17079247
ensemblrs17079247
gopubmedrs17079247
geneviewrs17079247
scholarrs17079247
googlers17079247
pharmgkbrs17079247
gwascentralrs17079247
openSNPrs17079247
23andMers17079247
23andMe allrs17079247
SNP Nexus

SNPshotrs17079247
SNPdbers17079247
MSV3drs17079247
GWAS Ctlgrs17079247
GMAF0.2626
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23326512OA-icon.png]
Trait Bipolar disorder (mania)
Title Genome-wide association study of irritable vs. elated mania suggests genetic differences between clinical subtypes of bipolar disorder.
Risk Allele T
P-val 8E-6
Odds Ratio 1.75