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rs4734782

From SNPedia

Orientationplus
Stabilizedplus
Make rs4734782(A;A)
Make rs4734782(A;C)
Make rs4734782(C;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position104362428
is asnp
is mentioned by
dbSNPrs4734782
ebirs4734782
HLIrs4734782
Exacrs4734782
Varsomers4734782
Maprs4734782
PheGenIrs4734782
hapmaprs4734782
1000 genomesrs4734782
hgdprs4734782
ensemblrs4734782
gopubmedrs4734782
geneviewrs4734782
scholarrs4734782
googlers4734782
pharmgkbrs4734782
gwascentralrs4734782
openSNPrs4734782
23andMers4734782
23andMe allrs4734782
SNP Nexus

SNPshotrs4734782
SNPdbers4734782
MSV3drs4734782
GWAS Ctlgrs4734782
GMAF0.4178
Max Magnitude
? (A;A) (A;C) (C;C) 28


GET Evidence
rs4734782
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.531746
summary