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rs17477949

From SNPedia

Orientationplus
Stabilizedplus
Make rs17477949(C;C)
Make rs17477949(C;T)
Make rs17477949(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position12197656
GeneMICAL2
is asnp
is mentioned by
dbSNPrs17477949
ebirs17477949
HLIrs17477949
Exacrs17477949
Varsomers17477949
Maprs17477949
PheGenIrs17477949
hapmaprs17477949
1000 genomesrs17477949
hgdprs17477949
ensemblrs17477949
gopubmedrs17477949
geneviewrs17477949
scholarrs17477949
googlers17477949
pharmgkbrs17477949
gwascentralrs17477949
openSNPrs17477949
23andMers17477949
23andMe allrs17477949
SNP Nexus

SNPshotrs17477949
SNPdbers17477949
MSV3drs17477949
GWAS Ctlgrs17477949
GMAF0.2107
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs17477949
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.261905
summary