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rs6972429

From SNPedia

Orientationplus
Stabilizedplus
Make rs6972429(C;C)
Make rs6972429(C;T)
Make rs6972429(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position41855244
is asnp
is mentioned by
dbSNPrs6972429
ebirs6972429
HLIrs6972429
Exacrs6972429
Varsomers6972429
Maprs6972429
PheGenIrs6972429
hapmaprs6972429
1000 genomesrs6972429
hgdprs6972429
ensemblrs6972429
gopubmedrs6972429
geneviewrs6972429
scholarrs6972429
googlers6972429
pharmgkbrs6972429
gwascentralrs6972429
openSNPrs6972429
23andMers6972429
23andMe allrs6972429
SNP Nexus

SNPshotrs6972429
SNPdbers6972429
MSV3drs6972429
GWAS Ctlgrs6972429
GMAF0.3926
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs6972429
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.653226
summary