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rs1131446

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1131446(A;A)
Make rs1131446(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355339
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1131446
ebirs1131446
HLIrs1131446
Exacrs1131446
Varsomers1131446
Maprs1131446
PheGenIrs1131446
hapmaprs1131446
1000 genomesrs1131446
hgdprs1131446
ensemblrs1131446
gopubmedrs1131446
geneviewrs1131446
scholarrs1131446
googlers1131446
pharmgkbrs1131446
gwascentralrs1131446
openSNPrs1131446
23andMers1131446
23andMe allrs1131446
SNP Nexus

SNPshotrs1131446
SNPdbers1131446
MSV3drs1131446
GWAS Ctlgrs1131446
GMAF0.03994
Max Magnitude0
ClinVar
Risk rs1131446(A;A)
Alt rs1131446(A;A)
Reference rs1131446(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323116C>T
CLNSRC
CLNACC