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rs3947413

From SNPedia

Orientationplus
Stabilizedplus
Make rs3947413(C;C)
Make rs3947413(C;T)
Make rs3947413(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position36547271
GeneFHOD3
is asnp
is mentioned by
dbSNPrs3947413
ebirs3947413
HLIrs3947413
Exacrs3947413
Varsomers3947413
Maprs3947413
PheGenIrs3947413
hapmaprs3947413
1000 genomesrs3947413
hgdprs3947413
ensemblrs3947413
gopubmedrs3947413
geneviewrs3947413
scholarrs3947413
googlers3947413
pharmgkbrs3947413
gwascentralrs3947413
openSNPrs3947413
23andMers3947413
23andMe allrs3947413
SNP Nexus

SNPshotrs3947413
SNPdbers3947413
MSV3drs3947413
GWAS Ctlgrs3947413
GMAF0.3994
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs3947413
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.421875
summary