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

rs2388449

From SNPedia

Orientationminus
Stabilizedminus
Make rs2388449(C;C)
Make rs2388449(C;T)
Make rs2388449(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position8444092
GeneSNORD19B
is asnp
is mentioned by
dbSNPrs2388449
ebirs2388449
HLIrs2388449
Exacrs2388449
Varsomers2388449
Maprs2388449
PheGenIrs2388449
hapmaprs2388449
1000 genomesrs2388449
hgdprs2388449
ensemblrs2388449
gopubmedrs2388449
geneviewrs2388449
scholarrs2388449
googlers2388449
pharmgkbrs2388449
gwascentralrs2388449
openSNPrs2388449
23andMers2388449
23andMe allrs2388449
SNP Nexus

SNPshotrs2388449
SNPdbers2388449
MSV3drs2388449
GWAS Ctlgrs2388449
GMAF0.3131
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs2388449
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.625
summary