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rs4690073

From SNPedia

Orientationplus
Stabilizedplus
Make rs4690073(A;A)
Make rs4690073(A;G)
Make rs4690073(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position3158423
GeneHTT
is asnp
is mentioned by
dbSNPrs4690073
ebirs4690073
HLIrs4690073
Exacrs4690073
Varsomers4690073
Maprs4690073
PheGenIrs4690073
hapmaprs4690073
1000 genomesrs4690073
hgdprs4690073
ensemblrs4690073
gopubmedrs4690073
geneviewrs4690073
scholarrs4690073
googlers4690073
pharmgkbrs4690073
gwascentralrs4690073
openSNPrs4690073
23andMers4690073
23andMe allrs4690073
SNP Nexus

SNPshotrs4690073
SNPdbers4690073
MSV3drs4690073
GWAS Ctlgrs4690073
GMAF0.4477
Max Magnitude
? (A;A) (A;G) (G;G) 28
GET Evidence
rs4690073
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.5
summary