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rs6942930

From SNPedia

Orientationplus
Stabilizedplus
Make rs6942930(A;A)
Make rs6942930(A;G)
Make rs6942930(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position1512784
is asnp
is mentioned by
dbSNPrs6942930
ebirs6942930
HLIrs6942930
Exacrs6942930
Varsomers6942930
Maprs6942930
PheGenIrs6942930
hapmaprs6942930
1000 genomesrs6942930
hgdprs6942930
ensemblrs6942930
gopubmedrs6942930
geneviewrs6942930
scholarrs6942930
googlers6942930
pharmgkbrs6942930
gwascentralrs6942930
openSNPrs6942930
23andMers6942930
23andMe allrs6942930
SNP Nexus

SNPshotrs6942930
SNPdbers6942930
MSV3drs6942930
GWAS Ctlgrs6942930
GMAF0.4541
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs6942930
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.484848
summary