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rs1574091

From SNPedia

Orientationplus
Stabilizedplus
Make rs1574091(C;C)
Make rs1574091(C;T)
Make rs1574091(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position192364293
GeneFGF12
is asnp
is mentioned by
dbSNPrs1574091
ebirs1574091
HLIrs1574091
Exacrs1574091
Varsomers1574091
Maprs1574091
PheGenIrs1574091
hapmaprs1574091
1000 genomesrs1574091
hgdprs1574091
ensemblrs1574091
gopubmedrs1574091
geneviewrs1574091
scholarrs1574091
googlers1574091
pharmgkbrs1574091
gwascentralrs1574091
openSNPrs1574091
23andMers1574091
23andMe allrs1574091
SNP Nexus

SNPshotrs1574091
SNPdbers1574091
MSV3drs1574091
GWAS Ctlgrs1574091
GMAF0.3884
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs1574091
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.34375
summary