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rs1542178

From SNPedia

Orientationminus
Stabilizedminus
Make rs1542178(C;C)
Make rs1542178(C;T)
Make rs1542178(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position100979013
GeneAC016738.3, NPAS2
is asnp
is mentioned by
dbSNPrs1542178
ebirs1542178
HLIrs1542178
Exacrs1542178
Varsomers1542178
Maprs1542178
PheGenIrs1542178
hapmaprs1542178
1000 genomesrs1542178
hgdprs1542178
ensemblrs1542178
gopubmedrs1542178
geneviewrs1542178
scholarrs1542178
googlers1542178
pharmgkbrs1542178
gwascentralrs1542178
openSNPrs1542178
23andMers1542178
23andMe allrs1542178
SNP Nexus

SNPshotrs1542178
SNPdbers1542178
MSV3drs1542178
GWAS Ctlgrs1542178
GMAF0.2355
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs1542178
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.819672
summary