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rs6744284

From SNPedia

Orientationplus
Stabilizedplus
Make rs6744284(C;C)
Make rs6744284(C;T)
Make rs6744284(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position233716651
GeneUGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs6744284
ebirs6744284
HLIrs6744284
Exacrs6744284
Varsomers6744284
Maprs6744284
PheGenIrs6744284
hapmaprs6744284
1000 genomesrs6744284
hgdprs6744284
ensemblrs6744284
gopubmedrs6744284
geneviewrs6744284
scholarrs6744284
googlers6744284
pharmgkbrs6744284
gwascentralrs6744284
openSNPrs6744284
23andMers6744284
23andMe allrs6744284
SNP Nexus

SNPshotrs6744284
SNPdbers6744284
MSV3drs6744284
GWAS Ctlgrs6744284
GMAF0.3297
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 22511988OA-icon.png] A Genome-Wide Association Study Identifies UGT1A1 as a Regulator of Serum Cell-Free DNA in Young Adults: The Cardiovascular Risk in Young Finns Study


[PMID 21291537OA-icon.png] Evidence for somatic gene conversion and deletion in bipolar disorder, Crohn's disease, coronary artery disease, hypertension, rheumatoid arthritis, type-1 diabetes, and type-2 diabetes.