Have questions? Visit https://www.reddit.com/r/SNPedia

rs17231520

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs17231520(A;A)
Make rs17231520(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position56961915
GeneCETP
is asnp
is mentioned by
dbSNPrs17231520
dbSNP (classic)rs17231520
ClinGenrs17231520
ebirs17231520
HLIrs17231520
Exacrs17231520
Gnomadrs17231520
Varsomers17231520
LitVarrs17231520
Maprs17231520
PheGenIrs17231520
Biobankrs17231520
1000 genomesrs17231520
hgdprs17231520
ensemblrs17231520
geneviewrs17231520
scholarrs17231520
googlers17231520
pharmgkbrs17231520
gwascentralrs17231520
openSNPrs17231520
23andMers17231520
SNPshotrs17231520
SNPdbers17231520
MSV3drs17231520
GWAS Ctlgrs17231520
GMAF0.01837
Max Magnitude0

[PMID 22539988OA-icon.png] Evaluation of the Metabochip Genotyping Array in African Americans and Implications for Fine Mapping of GWAS-Identified Loci: The PAGE Study


ClinVar
Risk rs17231520(A;A)
Alt rs17231520(A;A)
Reference Rs17231520(G;G)
Significance Non-pathogenic
Disease Hyperalphalipoproteinemia
Variation info
Gene CETP
CLNDBN Hyperalphalipoproteinemia
Reversed 0
HGVS NC_000016.9:g.56995827G>A
CLNSRC
CLNACC RCV000378884.1,