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rs41553818

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41553818(C;C)
Make rs41553818(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355489
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs41553818
dbSNP (classic)rs41553818
ClinGenrs41553818
ebirs41553818
HLIrs41553818
Exacrs41553818
Gnomadrs41553818
Varsomers41553818
LitVarrs41553818
Maprs41553818
PheGenIrs41553818
Biobankrs41553818
1000 genomesrs41553818
hgdprs41553818
ensemblrs41553818
geneviewrs41553818
scholarrs41553818
googlers41553818
pharmgkbrs41553818
gwascentralrs41553818
openSNPrs41553818
23andMers41553818
SNPshotrs41553818
SNPdbers41553818
MSV3drs41553818
GWAS Ctlgrs41553818
Max Magnitude0
ClinVar
Risk rs41553818(C;C)
Alt rs41553818(C;C)
Reference Rs41553818(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323266C>G
CLNSRC
CLNACC