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rs1035050

From SNPedia

Orientationplus
Stabilizedplus
Make rs1035050(C;C)
Make rs1035050(C;T)
Make rs1035050(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position49486650
is asnp
is mentioned by
dbSNPrs1035050
ebirs1035050
HLIrs1035050
Exacrs1035050
Varsomers1035050
Maprs1035050
PheGenIrs1035050
hapmaprs1035050
1000 genomesrs1035050
hgdprs1035050
ensemblrs1035050
gopubmedrs1035050
geneviewrs1035050
scholarrs1035050
googlers1035050
pharmgkbrs1035050
gwascentralrs1035050
openSNPrs1035050
23andMers1035050
23andMe allrs1035050
SNP Nexus

SNPshotrs1035050
SNPdbers1035050
MSV3drs1035050
GWAS Ctlgrs1035050
GMAF0.4261
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19416921OA-icon.png]
Trait Bipolar disorder
Title Genome-wide association and meta-analysis of

bipolar disorder in individuals of European ancestry

Risk Allele T
P-val 0.000009
Odds Ratio 1.17 [1.09-1.25]


GET Evidence
rs1035050
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.375
summary