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rs1036360

From SNPedia

Orientationplus
Stabilizedplus
Make rs1036360(A;A)
Make rs1036360(A;G)
Make rs1036360(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position94059553
is asnp
is mentioned by
dbSNPrs1036360
ebirs1036360
HLIrs1036360
Exacrs1036360
Varsomers1036360
Maprs1036360
PheGenIrs1036360
hapmaprs1036360
1000 genomesrs1036360
hgdprs1036360
ensemblrs1036360
gopubmedrs1036360
geneviewrs1036360
scholarrs1036360
googlers1036360
pharmgkbrs1036360
gwascentralrs1036360
openSNPrs1036360
23andMers1036360
23andMe allrs1036360
SNP Nexus

SNPshotrs1036360
SNPdbers1036360
MSV3drs1036360
GWAS Ctlgrs1036360
GMAF0.3659
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs1036360
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.390625
summary