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rs78536982

From SNPedia

Orientationplus
Stabilizedplus
Make rs78536982(C;C)
Make rs78536982(C;T)
Make rs78536982(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position69472818
is asnp
is mentioned by
dbSNPrs78536982
ebirs78536982
HLIrs78536982
Exacrs78536982
Varsomers78536982
Maprs78536982
PheGenIrs78536982
hapmaprs78536982
1000 genomesrs78536982
hgdprs78536982
ensemblrs78536982
gopubmedrs78536982
geneviewrs78536982
scholarrs78536982
googlers78536982
pharmgkbrs78536982
gwascentralrs78536982
openSNPrs78536982
23andMers78536982
23andMe allrs78536982
SNP Nexus

SNPshotrs78536982
SNPdbers78536982
MSV3drs78536982
GWAS Ctlgrs78536982
Max Magnitude
GWAS snp
PMID [PMID 24886709OA-icon.png]
Trait Triglycerides
Title Amerindian-specific regions under positive selection harbour new lipid variants in Latinos.
Risk Allele T
P-val 7E-9
Odds Ratio 1.38 [1.18–1.61]