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rs460106

From SNPedia

Orientationplus
Stabilizedplus
Make rs460106(C;C)
Make rs460106(C;T)
Make rs460106(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position21452112
GeneHIC2
is asnp
is mentioned by
dbSNPrs460106
ebirs460106
HLIrs460106
Exacrs460106
Varsomers460106
Maprs460106
PheGenIrs460106
hapmaprs460106
1000 genomesrs460106
hgdprs460106
ensemblrs460106
gopubmedrs460106
geneviewrs460106
scholarrs460106
googlers460106
pharmgkbrs460106
gwascentralrs460106
openSNPrs460106
23andMers460106
23andMe allrs460106
SNP Nexus

SNPshotrs460106
SNPdbers460106
MSV3drs460106
GWAS Ctlgrs460106
GMAF0.4555
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs460106
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.585938
summary