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rs2523605

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(G;G) 0 common in complete genomics
Make rs2523605(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355632
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2523605
ebirs2523605
HLIrs2523605
Exacrs2523605
Varsomers2523605
Maprs2523605
PheGenIrs2523605
hapmaprs2523605
1000 genomesrs2523605
hgdprs2523605
ensemblrs2523605
gopubmedrs2523605
geneviewrs2523605
scholarrs2523605
googlers2523605
pharmgkbrs2523605
gwascentralrs2523605
openSNPrs2523605
23andMers2523605
23andMe allrs2523605
SNP Nexus

SNPshotrs2523605
SNPdbers2523605
MSV3drs2523605
GWAS Ctlgrs2523605
GMAF0.1538
Max Magnitude0
? (A;A) (A;G) (G;G) 28
ClinVar
Risk rs2523605(G;G)
Alt rs2523605(G;G)
Reference rs2523605(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323409T>C
CLNSRC
CLNACC