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rs2159324

From SNPedia

Orientationplus
Stabilizedplus
Make rs2159324(C;C)
Make rs2159324(C;T)
Make rs2159324(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position45192480
is asnp
is mentioned by
dbSNPrs2159324
ebirs2159324
HLIrs2159324
Exacrs2159324
Varsomers2159324
Maprs2159324
PheGenIrs2159324
hapmaprs2159324
1000 genomesrs2159324
hgdprs2159324
ensemblrs2159324
gopubmedrs2159324
geneviewrs2159324
scholarrs2159324
googlers2159324
pharmgkbrs2159324
gwascentralrs2159324
openSNPrs2159324
23andMers2159324
23andMe allrs2159324
SNP Nexus

SNPshotrs2159324
SNPdbers2159324
MSV3drs2159324
GWAS Ctlgrs2159324
GMAF0.3315
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19197348OA-icon.png]
Trait Quantitative traits
Title Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
Risk Allele T
P-val 4E-7
Odds Ratio 0.21 [NR] mg/dL decrease

LDL cholesterol and total cholesterol levels being the quantitative trait associated with in [PMID 19197348OA-icon.png]


GET Evidence
rs2159324
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.333333
summary