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rs17157663

From SNPedia

Orientationplus
Stabilizedplus
Make rs17157663(A;A)
Make rs17157663(A;G)
Make rs17157663(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position8959346
is asnp
is mentioned by
dbSNPrs17157663
ebirs17157663
HLIrs17157663
Exacrs17157663
Varsomers17157663
Maprs17157663
PheGenIrs17157663
hapmaprs17157663
1000 genomesrs17157663
hgdprs17157663
ensemblrs17157663
gopubmedrs17157663
geneviewrs17157663
scholarrs17157663
googlers17157663
pharmgkbrs17157663
gwascentralrs17157663
openSNPrs17157663
23andMers17157663
23andMe allrs17157663
SNP Nexus

SNPshotrs17157663
SNPdbers17157663
MSV3drs17157663
GWAS Ctlgrs17157663
GMAF0.1919
Max Magnitude
? (A;A) (A;G) (G;G) 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 A
P-val 0.000009
Odds Ratio 0.18 [NR] mg/dL decrease

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


GET Evidence
rs17157663
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.125
summary