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rs2024115

From SNPedia

Orientationminus
Stabilizedminus
Make rs2024115(C;C)
Make rs2024115(C;T)
Make rs2024115(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position3102841
GeneHTT
is asnp
is mentioned by
dbSNPrs2024115
ebirs2024115
HLIrs2024115
Exacrs2024115
Varsomers2024115
Maprs2024115
PheGenIrs2024115
hapmaprs2024115
1000 genomesrs2024115
hgdprs2024115
ensemblrs2024115
gopubmedrs2024115
geneviewrs2024115
scholarrs2024115
googlers2024115
pharmgkbrs2024115
gwascentralrs2024115
openSNPrs2024115
23andMers2024115
23andMe allrs2024115
SNP Nexus

SNPshotrs2024115
SNPdbers2024115
MSV3drs2024115
GWAS Ctlgrs2024115
GMAF0.4027
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs2024115
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.429688
summary