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rs7187742

From SNPedia

Orientationplus
Stabilizedplus
Make rs7187742(C;C)
Make rs7187742(C;T)
Make rs7187742(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position60416342
is asnp
is mentioned by
dbSNPrs7187742
ebirs7187742
HLIrs7187742
Exacrs7187742
Varsomers7187742
Maprs7187742
PheGenIrs7187742
hapmaprs7187742
1000 genomesrs7187742
hgdprs7187742
ensemblrs7187742
gopubmedrs7187742
geneviewrs7187742
scholarrs7187742
googlers7187742
pharmgkbrs7187742
gwascentralrs7187742
openSNPrs7187742
23andMers7187742
23andMe allrs7187742
SNP Nexus

SNPshotrs7187742
SNPdbers7187742
MSV3drs7187742
GWAS Ctlgrs7187742
GMAF0.2782
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs7187742
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.710938
summary