Have questions? Visit https://www.reddit.com/r/SNPedia

rs12725861

From SNPedia

Orientationplus
Stabilizedplus
Make rs12725861(A;A)
Make rs12725861(A;G)
Make rs12725861(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position89100413
GeneLOC105378841
is asnp
is mentioned by
dbSNPrs12725861
dbSNP (old)rs12725861
ClinGenrs12725861
ebirs12725861
HLIrs12725861
Exacrs12725861
Gnomadrs12725861
Varsomers12725861
Maprs12725861
PheGenIrs12725861
Biobankrs12725861
1000 genomesrs12725861
hgdprs12725861
ensemblrs12725861
gopubmedrs12725861
geneviewrs12725861
scholarrs12725861
googlers12725861
pharmgkbrs12725861
gwascentralrs12725861
openSNPrs12725861
23andMers12725861
23andMe allrs12725861
SNP Nexus

SNPshotrs12725861
SNPdbers12725861
MSV3drs12725861
GWAS Ctlgrs12725861
GMAF0.3393
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs12725861
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.257812
summary