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

rs2222956

From SNPedia

Orientationminus
Stabilizedminus
Make rs2222956(C;C)
Make rs2222956(C;T)
Make rs2222956(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position35728742
is asnp
is mentioned by
dbSNPrs2222956
ebirs2222956
HLIrs2222956
Exacrs2222956
Varsomers2222956
Maprs2222956
PheGenIrs2222956
hapmaprs2222956
1000 genomesrs2222956
hgdprs2222956
ensemblrs2222956
gopubmedrs2222956
geneviewrs2222956
scholarrs2222956
googlers2222956
pharmgkbrs2222956
gwascentralrs2222956
openSNPrs2222956
23andMers2222956
23andMe allrs2222956
SNP Nexus

SNPshotrs2222956
SNPdbers2222956
MSV3drs2222956
GWAS Ctlgrs2222956
GMAF0.4362
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs2222956
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.492188
summary