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rs16889859

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs16889859(A;G)
Make rs16889859(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position78316148
is asnp
is mentioned by
dbSNPrs16889859
ebirs16889859
HLIrs16889859
Exacrs16889859
Varsomers16889859
Maprs16889859
PheGenIrs16889859
hapmaprs16889859
1000 genomesrs16889859
hgdprs16889859
ensemblrs16889859
gopubmedrs16889859
geneviewrs16889859
scholarrs16889859
googlers16889859
pharmgkbrs16889859
gwascentralrs16889859
openSNPrs16889859
23andMers16889859
23andMe allrs16889859
SNP Nexus

SNPshotrs16889859
SNPdbers16889859
MSV3drs16889859
GWAS Ctlgrs16889859
GMAF0.0955
Max Magnitude0
? (A;A) (A;G) (G;G) 28
Here to enable genosets gs217 and gs218 which look for a CNV