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rs2394985

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2394985(C;T)
Make rs2394985(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355780
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2394985
ebirs2394985
HLIrs2394985
Exacrs2394985
Varsomers2394985
Maprs2394985
PheGenIrs2394985
hapmaprs2394985
1000 genomesrs2394985
hgdprs2394985
ensemblrs2394985
gopubmedrs2394985
geneviewrs2394985
scholarrs2394985
googlers2394985
pharmgkbrs2394985
gwascentralrs2394985
openSNPrs2394985
23andMers2394985
23andMe allrs2394985
SNP Nexus

SNPshotrs2394985
SNPdbers2394985
MSV3drs2394985
GWAS Ctlgrs2394985
GMAF0.0124
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs2394985(T;T)
Alt rs2394985(T;T)
Reference rs2394985(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31323557C>T
CLNSRC
CLNACC