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rs148982608

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs148982608(A;A)
Make rs148982608(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355561
GeneHLA-B
is asnp
is mentioned by
dbSNPrs148982608
ebirs148982608
HLIrs148982608
Exacrs148982608
Varsomers148982608
Maprs148982608
PheGenIrs148982608
hapmaprs148982608
1000 genomesrs148982608
hgdprs148982608
ensemblrs148982608
gopubmedrs148982608
geneviewrs148982608
scholarrs148982608
googlers148982608
pharmgkbrs148982608
gwascentralrs148982608
openSNPrs148982608
23andMers148982608
23andMe allrs148982608
SNP Nexus

SNPshotrs148982608
SNPdbers148982608
MSV3drs148982608
GWAS Ctlgrs148982608
Max Magnitude0
ClinVar
Risk rs148982608(A;A)
Alt rs148982608(A;A)
Reference rs148982608(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31323338G>A
CLNSRC
CLNACC