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rs12190776

From SNPedia

Orientationplus
Stabilizedplus
Make rs12190776(C;C)
Make rs12190776(C;G)
Make rs12190776(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position123981398
GeneNKAIN2
is asnp
is mentioned by
dbSNPrs12190776
ebirs12190776
HLIrs12190776
Exacrs12190776
Varsomers12190776
Maprs12190776
PheGenIrs12190776
hapmaprs12190776
1000 genomesrs12190776
hgdprs12190776
ensemblrs12190776
gopubmedrs12190776
geneviewrs12190776
scholarrs12190776
googlers12190776
pharmgkbrs12190776
gwascentralrs12190776
openSNPrs12190776
23andMers12190776
23andMe allrs12190776
SNP Nexus

SNPshotrs12190776
SNPdbers12190776
MSV3drs12190776
GWAS Ctlgrs12190776
GMAF0.2236
Max Magnitude
? (C;C) (C;G) (G;G) 28


GET Evidence
rs12190776
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.234375
summary