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rs2523607

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2523607(A;T)
Make rs2523607(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355013
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2523607
ebirs2523607
HLIrs2523607
Exacrs2523607
Varsomers2523607
Maprs2523607
PheGenIrs2523607
hapmaprs2523607
1000 genomesrs2523607
hgdprs2523607
ensemblrs2523607
gopubmedrs2523607
geneviewrs2523607
scholarrs2523607
googlers2523607
pharmgkbrs2523607
gwascentralrs2523607
openSNPrs2523607
23andMers2523607
23andMe allrs2523607
SNP Nexus

SNPshotrs2523607
SNPdbers2523607
MSV3drs2523607
GWAS Ctlgrs2523607
GMAF0.07117
Max Magnitude0
ClinVar
Risk rs2523607(T;T)
Alt rs2523607(T;T)
Reference rs2523607(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322790T>A
CLNSRC
CLNACC