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rs2298967

From SNPedia

Orientationplus
Stabilizedplus
Make rs2298967(C;C)
Make rs2298967(C;T)
Make rs2298967(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position3184020
GeneHTT
is asnp
is mentioned by
dbSNPrs2298967
ebirs2298967
HLIrs2298967
Exacrs2298967
Varsomers2298967
Maprs2298967
PheGenIrs2298967
hapmaprs2298967
1000 genomesrs2298967
hgdprs2298967
ensemblrs2298967
gopubmedrs2298967
geneviewrs2298967
scholarrs2298967
googlers2298967
pharmgkbrs2298967
gwascentralrs2298967
openSNPrs2298967
23andMers2298967
23andMe allrs2298967
SNP Nexus

SNPshotrs2298967
SNPdbers2298967
MSV3drs2298967
GWAS Ctlgrs2298967
GMAF0.2626
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs2298967
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.265625
summary