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rs41555514

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41555514(A;C)
Make rs41555514(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355162
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs41555514
dbSNP (classic)rs41555514
ClinGenrs41555514
ebirs41555514
HLIrs41555514
Exacrs41555514
Gnomadrs41555514
Varsomers41555514
LitVarrs41555514
Maprs41555514
PheGenIrs41555514
Biobankrs41555514
1000 genomesrs41555514
hgdprs41555514
ensemblrs41555514
geneviewrs41555514
scholarrs41555514
googlers41555514
pharmgkbrs41555514
gwascentralrs41555514
openSNPrs41555514
23andMers41555514
SNPshotrs41555514
SNPdbers41555514
MSV3drs41555514
GWAS Ctlgrs41555514
Max Magnitude0
ClinVar
Risk rs41555514(C;C)
Alt rs41555514(C;C)
Reference Rs41555514(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322939T>G
CLNSRC
CLNACC