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rs11244841

From SNPedia

Orientationplus
Stabilizedplus
Make rs11244841(C;C)
Make rs11244841(C;T)
Make rs11244841(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position126145997
GeneADAM12
is asnp
is mentioned by
dbSNPrs11244841
ebirs11244841
HLIrs11244841
Exacrs11244841
Varsomers11244841
Maprs11244841
PheGenIrs11244841
hapmaprs11244841
1000 genomesrs11244841
hgdprs11244841
ensemblrs11244841
gopubmedrs11244841
geneviewrs11244841
scholarrs11244841
googlers11244841
pharmgkbrs11244841
gwascentralrs11244841
openSNPrs11244841
23andMers11244841
23andMe allrs11244841
SNP Nexus

SNPshotrs11244841
SNPdbers11244841
MSV3drs11244841
GWAS Ctlgrs11244841
GMAF0.191
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs11244841
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.15625
summary