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Rs2844682

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Orientationminus
Geno Mag Summary
(C;C) 0 common in complete genomics
(T;T) 3
Make rs2844682(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position30978371
is asnp
is mentioned by
dbSNPrs2844682
PheGenIrs2844682
nextbiors2844682
hapmaprs2844682
1000 genomesrs2844682
hgdprs2844682
ensemblrs2844682
gopubmedrs2844682
geneviewrs2844682
scholarrs2844682
googlers2844682
pharmgkbrs2844682
gwascentralrs2844682
openSNPrs2844682
23andMers2844682
23andMe allrs2844682
SNP Nexus

SNPshotrs2844682
SNPdbers2844682
MSV3drs2844682
GMAF0.1515
Max Magnitude3
? (C;C) (C;T) (T;T) 28

Helps to identify HLA-B*1502




GET Evidence
rs2844682
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.164062
summary