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rs6851702

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs6851702(A;G)
Make rs6851702(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position27054735
is asnp
is mentioned by
dbSNPrs6851702
ebirs6851702
HLIrs6851702
Exacrs6851702
Varsomers6851702
Maprs6851702
PheGenIrs6851702
hapmaprs6851702
1000 genomesrs6851702
hgdprs6851702
ensemblrs6851702
gopubmedrs6851702
geneviewrs6851702
scholarrs6851702
googlers6851702
pharmgkbrs6851702
gwascentralrs6851702
openSNPrs6851702
23andMers6851702
23andMe allrs6851702
SNP Nexus

SNPshotrs6851702
SNPdbers6851702
MSV3drs6851702
GWAS Ctlgrs6851702
GMAF0.1924
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GET Evidence
rs6851702
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.179688
summary