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rs10794595

From SNPedia

Orientationplus
Stabilizedplus
Make rs10794595(C;C)
Make rs10794595(C;T)
Make rs10794595(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position123121986
is asnp
is mentioned by
dbSNPrs10794595
ebirs10794595
HLIrs10794595
Exacrs10794595
Varsomers10794595
Maprs10794595
PheGenIrs10794595
hapmaprs10794595
1000 genomesrs10794595
hgdprs10794595
ensemblrs10794595
gopubmedrs10794595
geneviewrs10794595
scholarrs10794595
googlers10794595
pharmgkbrs10794595
gwascentralrs10794595
openSNPrs10794595
23andMers10794595
23andMe allrs10794595
SNP Nexus

SNPshotrs10794595
SNPdbers10794595
MSV3drs10794595
GWAS Ctlgrs10794595
GMAF0.3039
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs10794595
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.65625
summary