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rs1143646

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs1143646(G;G)
Make rs1143646(G;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position3146926
GeneHTT
is asnp
is mentioned by
dbSNPrs1143646
ebirs1143646
HLIrs1143646
Exacrs1143646
Varsomers1143646
Maprs1143646
PheGenIrs1143646
hapmaprs1143646
1000 genomesrs1143646
hgdprs1143646
ensemblrs1143646
gopubmedrs1143646
geneviewrs1143646
scholarrs1143646
googlers1143646
pharmgkbrs1143646
gwascentralrs1143646
openSNPrs1143646
23andMers1143646
23andMe allrs1143646
SNP Nexus

SNPshotrs1143646
SNPdbers1143646
MSV3drs1143646
GWAS Ctlgrs1143646
Merged fromRs17781557
GMAF0.02296
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 19361997OA-icon.png] Five siRNAs targeting three SNPs may provide therapy for three-quarters of Huntington's disease patients.
GET Evidence
HTT-I1091M
aa_change Ile1091Met
aa_change_short I1091M
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0352776
summary