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rs3856973

From SNPedia

Orientationminus
Stabilizedminus
Make rs3856973(C;C)
Make rs3856973(C;T)
Make rs3856973(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position3078446
GeneHTT
is asnp
is mentioned by
dbSNPrs3856973
ebirs3856973
HLIrs3856973
Exacrs3856973
Varsomers3856973
Maprs3856973
PheGenIrs3856973
hapmaprs3856973
1000 genomesrs3856973
hgdprs3856973
ensemblrs3856973
gopubmedrs3856973
geneviewrs3856973
scholarrs3856973
googlers3856973
pharmgkbrs3856973
gwascentralrs3856973
openSNPrs3856973
23andMers3856973
23andMe allrs3856973
SNP Nexus

SNPshotrs3856973
SNPdbers3856973
MSV3drs3856973
GWAS Ctlgrs3856973
GMAF0.4302
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs3856973
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.460938
summary