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rs2857936

From SNPedia

Orientationminus
Stabilizedminus
Make rs2857936(A;A)
Make rs2857936(A;G)
Make rs2857936(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position3060583
is asnp
is mentioned by
dbSNPrs2857936
ebirs2857936
HLIrs2857936
Exacrs2857936
Varsomers2857936
Maprs2857936
PheGenIrs2857936
hapmaprs2857936
1000 genomesrs2857936
hgdprs2857936
ensemblrs2857936
gopubmedrs2857936
geneviewrs2857936
scholarrs2857936
googlers2857936
pharmgkbrs2857936
gwascentralrs2857936
openSNPrs2857936
23andMers2857936
23andMe allrs2857936
SNP Nexus

SNPshotrs2857936
SNPdbers2857936
MSV3drs2857936
GWAS Ctlgrs2857936
GMAF0.4752
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs2857936
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.523438
summary