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rs6698843

From SNPedia

Orientationplus
Make rs6698843(C;C)
Make rs6698843(C;T)
Make rs6698843(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position109264212
GeneCELSR2
is asnp
is mentioned by
dbSNPrs6698843
ebirs6698843
HLIrs6698843
Exacrs6698843
Varsomers6698843
Maprs6698843
PheGenIrs6698843
hapmaprs6698843
1000 genomesrs6698843
hgdprs6698843
ensemblrs6698843
gopubmedrs6698843
geneviewrs6698843
scholarrs6698843
googlers6698843
pharmgkbrs6698843
gwascentralrs6698843
openSNPrs6698843
23andMers6698843
23andMe allrs6698843
SNP Nexus

SNPshotrs6698843
SNPdbers6698843
MSV3drs6698843
GWAS Ctlgrs6698843
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 26464717OA-icon.png] Association of variants in CELSR2-PSRC1-SORT1 with risk of serum lipid traits, coronary artery disease and ischemic stroke