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rs17216525

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17216525(C;T)
Make rs17216525(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position19551411
is asnp
is mentioned by
dbSNPrs17216525
ebirs17216525
HLIrs17216525
Exacrs17216525
Varsomers17216525
Maprs17216525
PheGenIrs17216525
hapmaprs17216525
1000 genomesrs17216525
hgdprs17216525
ensemblrs17216525
gopubmedrs17216525
geneviewrs17216525
scholarrs17216525
googlers17216525
pharmgkbrs17216525
gwascentralrs17216525
openSNPrs17216525
23andMers17216525
23andMe allrs17216525
SNP Nexus

SNPshotrs17216525
SNPdbers17216525
MSV3drs17216525
GWAS Ctlgrs17216525
GMAF0.07117
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19060906OA-icon.png]
Trait Triglycerides
Title Common variants at 30 loci contribute to polygenic dyslipidemia
Risk Allele T
P-val 4E-11
Odds Ratio 0.11 [0.05-0.17] SD decrease



GET Evidence
rs17216525
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.09375
summary