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rs7784162

From SNPedia

Orientationplus
Stabilizedplus
Make rs7784162(A;A)
Make rs7784162(A;C)
Make rs7784162(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position135621138
GeneNUP205
is asnp
is mentioned by
dbSNPrs7784162
ebirs7784162
HLIrs7784162
Exacrs7784162
Varsomers7784162
Maprs7784162
PheGenIrs7784162
hapmaprs7784162
1000 genomesrs7784162
hgdprs7784162
ensemblrs7784162
gopubmedrs7784162
geneviewrs7784162
scholarrs7784162
googlers7784162
pharmgkbrs7784162
gwascentralrs7784162
openSNPrs7784162
23andMers7784162
23andMe allrs7784162
SNP Nexus

SNPshotrs7784162
SNPdbers7784162
MSV3drs7784162
GWAS Ctlgrs7784162
GMAF0.2502
Max Magnitude
? (A;A) (A;C) (C;C) 28


GET Evidence
rs7784162
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.25
summary