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rs983579

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs983579(C;C)
Make rs983579(C;T)
Make rs983579(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position32991864
is asnp
is mentioned by
dbSNPrs983579
ebirs983579
HLIrs983579
Exacrs983579
Varsomers983579
Maprs983579
PheGenIrs983579
hapmaprs983579
1000 genomesrs983579
hgdprs983579
ensemblrs983579
gopubmedrs983579
geneviewrs983579
scholarrs983579
googlers983579
pharmgkbrs983579
gwascentralrs983579
openSNPrs983579
23andMers983579
23andMe allrs983579
SNP Nexus

SNPshotrs983579
SNPdbers983579
MSV3drs983579
GWAS Ctlgrs983579
GMAF0.04637
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs983579
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0564516
summary