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

rs1993508

From SNPedia

Orientationplus
Stabilizedplus
Make rs1993508(C;C)
Make rs1993508(C;G)
Make rs1993508(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position13379397
is asnp
is mentioned by
dbSNPrs1993508
ebirs1993508
HLIrs1993508
Exacrs1993508
Varsomers1993508
Maprs1993508
PheGenIrs1993508
hapmaprs1993508
1000 genomesrs1993508
hgdprs1993508
ensemblrs1993508
gopubmedrs1993508
geneviewrs1993508
scholarrs1993508
googlers1993508
pharmgkbrs1993508
gwascentralrs1993508
openSNPrs1993508
23andMers1993508
23andMe allrs1993508
SNP Nexus

SNPshotrs1993508
SNPdbers1993508
MSV3drs1993508
GWAS Ctlgrs1993508
GMAF0.3563
Max Magnitude
? (C;C) (C;G) (G;G) 28


GET Evidence
rs1993508
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.242188
summary