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rs6080699

From SNPedia

Orientationplus
Stabilizedplus
Make rs6080699(C;C)
Make rs6080699(C;G)
Make rs6080699(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position17453641
GenePCSK2
is asnp
is mentioned by
dbSNPrs6080699
ebirs6080699
HLIrs6080699
Exacrs6080699
Varsomers6080699
Maprs6080699
PheGenIrs6080699
hapmaprs6080699
1000 genomesrs6080699
hgdprs6080699
ensemblrs6080699
gopubmedrs6080699
geneviewrs6080699
scholarrs6080699
googlers6080699
pharmgkbrs6080699
gwascentralrs6080699
openSNPrs6080699
23andMers6080699
23andMe allrs6080699
SNP Nexus

SNPshotrs6080699
SNPdbers6080699
MSV3drs6080699
GWAS Ctlgrs6080699
GMAF0.2493
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 20036365] Association of genetic variants in SEMA3F, CLEC16A, LAMA3, and PCSK2 with myocardial infarction in Japanese individuals