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rs1596725

From SNPedia

Orientationplus
Stabilizedplus
Make rs1596725(A;A)
Make rs1596725(A;C)
Make rs1596725(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position65028591
is asnp
is mentioned by
dbSNPrs1596725
ebirs1596725
HLIrs1596725
Exacrs1596725
Varsomers1596725
Maprs1596725
PheGenIrs1596725
hapmaprs1596725
1000 genomesrs1596725
hgdprs1596725
ensemblrs1596725
gopubmedrs1596725
geneviewrs1596725
scholarrs1596725
googlers1596725
pharmgkbrs1596725
gwascentralrs1596725
openSNPrs1596725
23andMers1596725
23andMe allrs1596725
SNP Nexus

SNPshotrs1596725
SNPdbers1596725
MSV3drs1596725
GWAS Ctlgrs1596725
GMAF0.3343
Max Magnitude
? (A;A) (A;C) (C;C) 28


GET Evidence
rs1596725
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.3125
summary