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rs29684

From SNPedia

Orientationminus
Stabilizedminus
Make rs29684(C;C)
Make rs29684(C;T)
Make rs29684(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position41815054
is asnp
is mentioned by
dbSNPrs29684
ebirs29684
HLIrs29684
Exacrs29684
Varsomers29684
Maprs29684
PheGenIrs29684
hapmaprs29684
1000 genomesrs29684
hgdprs29684
ensemblrs29684
gopubmedrs29684
geneviewrs29684
scholarrs29684
googlers29684
pharmgkbrs29684
gwascentralrs29684
openSNPrs29684
23andMers29684
23andMe allrs29684
SNP Nexus

SNPshotrs29684
SNPdbers29684
MSV3drs29684
GWAS Ctlgrs29684
GMAF0.3026
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs29684
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.320312
summary