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rs6576629

From SNPedia

Orientationplus
Stabilizedplus
Make rs6576629(A;A)
Make rs6576629(A;C)
Make rs6576629(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position26820960
is asnp
is mentioned by
dbSNPrs6576629
ebirs6576629
HLIrs6576629
Exacrs6576629
Varsomers6576629
Maprs6576629
PheGenIrs6576629
hapmaprs6576629
1000 genomesrs6576629
hgdprs6576629
ensemblrs6576629
gopubmedrs6576629
geneviewrs6576629
scholarrs6576629
googlers6576629
pharmgkbrs6576629
gwascentralrs6576629
openSNPrs6576629
23andMers6576629
23andMe allrs6576629
SNP Nexus

SNPshotrs6576629
SNPdbers6576629
MSV3drs6576629
GWAS Ctlgrs6576629
GMAF0.1639
Max Magnitude

[PMID 23707316] High intestinal cholesterol absorption is associated with cardiovascular disease and risk alleles in ABCG8 and ABO: evidence from the LURIC and YFS cohorts and from a meta-analysis