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rs1373494

From SNPedia

Orientationplus
Stabilizedplus
Make rs1373494(A;A)
Make rs1373494(A;C)
Make rs1373494(C;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position33746904
is asnp
is mentioned by
dbSNPrs1373494
ebirs1373494
HLIrs1373494
Exacrs1373494
Varsomers1373494
Maprs1373494
PheGenIrs1373494
hapmaprs1373494
1000 genomesrs1373494
hgdprs1373494
ensemblrs1373494
gopubmedrs1373494
geneviewrs1373494
scholarrs1373494
googlers1373494
pharmgkbrs1373494
gwascentralrs1373494
openSNPrs1373494
23andMers1373494
23andMe allrs1373494
SNP Nexus

SNPshotrs1373494
SNPdbers1373494
MSV3drs1373494
GWAS Ctlgrs1373494
GMAF0.264
Max Magnitude
? (A;A) (A;C) (C;C) 28
[PMID 18205893OA-icon.png] Study of regions of extended homozygosity provides a powerful method to explore haplotype structure of human populations.


GET Evidence
rs1373494
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.265625
summary