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rs6109332

From SNPedia

Orientationplus
Make rs6109332(A;A)
Make rs6109332(A;G)
Make rs6109332(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position12271830
is asnp
is mentioned by
dbSNPrs6109332
ebirs6109332
HLIrs6109332
Exacrs6109332
Varsomers6109332
Maprs6109332
PheGenIrs6109332
hapmaprs6109332
1000 genomesrs6109332
hgdprs6109332
ensemblrs6109332
gopubmedrs6109332
geneviewrs6109332
scholarrs6109332
googlers6109332
pharmgkbrs6109332
gwascentralrs6109332
openSNPrs6109332
23andMers6109332
23andMe allrs6109332
SNP Nexus

SNPshotrs6109332
SNPdbers6109332
MSV3drs6109332
GWAS Ctlgrs6109332
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 27103528] Association of genetic risk factors with cognitive decline: the PATH through life project.