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rs2257269

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2257269(C;T)
Make rs2257269(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355576
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2257269
ebirs2257269
HLIrs2257269
Exacrs2257269
Varsomers2257269
Maprs2257269
PheGenIrs2257269
hapmaprs2257269
1000 genomesrs2257269
hgdprs2257269
ensemblrs2257269
gopubmedrs2257269
geneviewrs2257269
scholarrs2257269
googlers2257269
pharmgkbrs2257269
gwascentralrs2257269
openSNPrs2257269
23andMers2257269
23andMe allrs2257269
SNP Nexus

SNPshotrs2257269
SNPdbers2257269
MSV3drs2257269
GWAS Ctlgrs2257269
GMAF0.3898
Max Magnitude0
ClinVar
Risk rs2257269(T;T)
Alt rs2257269(T;T)
Reference rs2257269(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323353G>A
CLNSRC
CLNACC