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rs6960379

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6960379(C;C)
Make rs6960379(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position64290139
is asnp
is mentioned by
dbSNPrs6960379
ebirs6960379
HLIrs6960379
Exacrs6960379
Varsomers6960379
Maprs6960379
PheGenIrs6960379
hapmaprs6960379
1000 genomesrs6960379
hgdprs6960379
ensemblrs6960379
gopubmedrs6960379
geneviewrs6960379
scholarrs6960379
googlers6960379
pharmgkbrs6960379
gwascentralrs6960379
openSNPrs6960379
23andMers6960379
23andMe allrs6960379
SNP Nexus

SNPshotrs6960379
SNPdbers6960379
MSV3drs6960379
GWAS Ctlgrs6960379
GMAF0.1244
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs6960379
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.179688
summary