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rs41545916

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41545916(A;G)
Make rs41545916(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355425
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs41545916
dbSNP (classic)rs41545916
ClinGenrs41545916
ebirs41545916
HLIrs41545916
Exacrs41545916
Gnomadrs41545916
Varsomers41545916
LitVarrs41545916
Maprs41545916
PheGenIrs41545916
Biobankrs41545916
1000 genomesrs41545916
hgdprs41545916
ensemblrs41545916
geneviewrs41545916
scholarrs41545916
googlers41545916
pharmgkbrs41545916
gwascentralrs41545916
openSNPrs41545916
23andMers41545916
SNPshotrs41545916
SNPdbers41545916
MSV3drs41545916
GWAS Ctlgrs41545916
Max Magnitude0
ClinVar
Risk rs41545916(G;G)
Alt rs41545916(G;G)
Reference Rs41545916(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323202T>C
CLNSRC
CLNACC