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rs7691996

From SNPedia

Orientationplus
Stabilizedplus
Make rs7691996(A;A)
Make rs7691996(A;G)
Make rs7691996(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position33728154
is asnp
is mentioned by
dbSNPrs7691996
ebirs7691996
HLIrs7691996
Exacrs7691996
Varsomers7691996
Maprs7691996
PheGenIrs7691996
hapmaprs7691996
1000 genomesrs7691996
hgdprs7691996
ensemblrs7691996
gopubmedrs7691996
geneviewrs7691996
scholarrs7691996
googlers7691996
pharmgkbrs7691996
gwascentralrs7691996
openSNPrs7691996
23andMers7691996
23andMe allrs7691996
SNP Nexus

SNPshotrs7691996
SNPdbers7691996
MSV3drs7691996
GWAS Ctlgrs7691996
GMAF0.2658
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs7691996
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.261905
summary