Have questions? Visit https://www.reddit.com/r/SNPedia

rs2119067

From SNPedia

Orientationminus
Stabilizedminus
Make rs2119067(A;A)
Make rs2119067(A;G)
Make rs2119067(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position165270773
GeneSCN2A
is asnp
is mentioned by
dbSNPrs2119067
dbSNP (old)rs2119067
ClinGenrs2119067
ebirs2119067
HLIrs2119067
Exacrs2119067
Gnomadrs2119067
Varsomers2119067
Maprs2119067
PheGenIrs2119067
Biobankrs2119067
1000 genomesrs2119067
hgdprs2119067
ensemblrs2119067
gopubmedrs2119067
geneviewrs2119067
scholarrs2119067
googlers2119067
pharmgkbrs2119067
gwascentralrs2119067
openSNPrs2119067
23andMers2119067
23andMe allrs2119067
SNP Nexus

SNPshotrs2119067
SNPdbers2119067
MSV3drs2119067
GWAS Ctlgrs2119067
GMAF0.2016
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs2119067
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.835938
summary