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rs4142237

From SNPedia

Orientationplus
Stabilizedplus
Make rs4142237(A;A)
Make rs4142237(A;G)
Make rs4142237(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position10390424
GeneHPCAL1
is asnp
is mentioned by
dbSNPrs4142237
ebirs4142237
HLIrs4142237
Exacrs4142237
Varsomers4142237
Maprs4142237
PheGenIrs4142237
hapmaprs4142237
1000 genomesrs4142237
hgdprs4142237
ensemblrs4142237
gopubmedrs4142237
geneviewrs4142237
scholarrs4142237
googlers4142237
pharmgkbrs4142237
gwascentralrs4142237
openSNPrs4142237
23andMers4142237
23andMe allrs4142237
SNP Nexus

SNPshotrs4142237
SNPdbers4142237
MSV3drs4142237
GWAS Ctlgrs4142237
GMAF0.3714
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs4142237
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.296875
summary