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rs7893928

From SNPedia

Orientationplus
Stabilizedplus
Make rs7893928(C;C)
Make rs7893928(C;T)
Make rs7893928(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position44583495
is asnp
is mentioned by
dbSNPrs7893928
ebirs7893928
HLIrs7893928
Exacrs7893928
Varsomers7893928
Maprs7893928
PheGenIrs7893928
hapmaprs7893928
1000 genomesrs7893928
hgdprs7893928
ensemblrs7893928
gopubmedrs7893928
geneviewrs7893928
scholarrs7893928
googlers7893928
pharmgkbrs7893928
gwascentralrs7893928
openSNPrs7893928
23andMers7893928
23andMe allrs7893928
SNP Nexus

SNPshotrs7893928
SNPdbers7893928
MSV3drs7893928
GWAS Ctlgrs7893928
GMAF0.0932
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs7893928
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.109375
summary