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rs41547514

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41547514(A;G)
Make rs41547514(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354979
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs41547514
dbSNP (classic)rs41547514
ClinGenrs41547514
ebirs41547514
HLIrs41547514
Exacrs41547514
Gnomadrs41547514
Varsomers41547514
LitVarrs41547514
Maprs41547514
PheGenIrs41547514
Biobankrs41547514
1000 genomesrs41547514
hgdprs41547514
ensemblrs41547514
geneviewrs41547514
scholarrs41547514
googlers41547514
pharmgkbrs41547514
gwascentralrs41547514
openSNPrs41547514
23andMers41547514
SNPshotrs41547514
SNPdbers41547514
MSV3drs41547514
GWAS Ctlgrs41547514
Max Magnitude0
ClinVar
Risk rs41547514(G;G)
Alt rs41547514(G;G)
Reference Rs41547514(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322756T>C
CLNSRC
CLNACC