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rs79236614

From SNPedia

Orientationplus
Stabilizedplus
Make rs79236614(C;C)
Make rs79236614(C;G)
Make rs79236614(G;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position20002949
is asnp
is mentioned by
dbSNPrs79236614
ebirs79236614
HLIrs79236614
Exacrs79236614
Varsomers79236614
Maprs79236614
PheGenIrs79236614
hapmaprs79236614
1000 genomesrs79236614
hgdprs79236614
ensemblrs79236614
gopubmedrs79236614
geneviewrs79236614
scholarrs79236614
googlers79236614
pharmgkbrs79236614
gwascentralrs79236614
openSNPrs79236614
23andMers79236614
23andMe allrs79236614
SNP Nexus

SNPshotrs79236614
SNPdbers79236614
MSV3drs79236614
GWAS Ctlgrs79236614
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
P-val 7E-9
Odds Ratio 1.89 [1.49-2.38]