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rs362272

From SNPedia

Orientationminus
Stabilizedminus
Make rs362272(C;C)
Make rs362272(C;T)
Make rs362272(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position3233253
GeneHTT
is asnp
is mentioned by
dbSNPrs362272
ebirs362272
HLIrs362272
Exacrs362272
Varsomers362272
Maprs362272
PheGenIrs362272
hapmaprs362272
1000 genomesrs362272
hgdprs362272
ensemblrs362272
gopubmedrs362272
geneviewrs362272
scholarrs362272
googlers362272
pharmgkbrs362272
gwascentralrs362272
openSNPrs362272
23andMers362272
23andMe allrs362272
SNP Nexus

SNPshotrs362272
SNPdbers362272
MSV3drs362272
GWAS Ctlgrs362272
GMAF0.2466
Max Magnitude
? (C;C) (C;T) (T;T) 28


[PMID 19115052] Common variations in 4p locus are related to male completed suicide.


[PMID 19361997OA-icon.png] Five siRNAs targeting three SNPs may provide therapy for three-quarters of Huntington's disease patients.


GET Evidence
HTT-V2786I
aa_change Val2786Ile
aa_change_short V2786I
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.215611
summary