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rs2844682

From SNPedia

Orientationminus
Stabilizedminus
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
dbSNP (classic)rs2844682
ClinGenrs2844682
ebirs2844682
HLIrs2844682
Exacrs2844682
Gnomadrs2844682
Varsomers2844682
LitVarrs2844682
Maprs2844682
PheGenIrs2844682
Biobankrs2844682
1000 genomesrs2844682
hgdprs2844682
ensemblrs2844682
geneviewrs2844682
scholarrs2844682
googlers2844682
pharmgkbrs2844682
gwascentralrs2844682
openSNPrs2844682
23andMers2844682
SNPshotrs2844682
SNPdbers2844682
MSV3drs2844682
GWAS Ctlgrs2844682
GMAF0.1515
Max Magnitude3
? (C;C) (C;T) (T;T) 28


Helps to identify HLA-B*1502