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rs2284018

From SNPedia

Orientationplus
Stabilizedplus
Make rs2284018(C;C)
Make rs2284018(C;T)
Make rs2284018(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position36701519
GeneCACNG2
is asnp
is mentioned by
dbSNPrs2284018
ebirs2284018
HLIrs2284018
Exacrs2284018
Varsomers2284018
Maprs2284018
PheGenIrs2284018
hapmaprs2284018
1000 genomesrs2284018
hgdprs2284018
ensemblrs2284018
gopubmedrs2284018
geneviewrs2284018
scholarrs2284018
googlers2284018
pharmgkbrs2284018
gwascentralrs2284018
openSNPrs2284018
23andMers2284018
23andMe allrs2284018
SNP Nexus

SNPshotrs2284018
SNPdbers2284018
MSV3drs2284018
GWAS Ctlgrs2284018
GMAF0.2525
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs2284018
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.230159
summary



[PMID 24581832] Exploring the associations between genetic variants in genes encoding for subunits of calcium channel and subtypes of bipolar disorder