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rs41558514

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41558514(A;A)
Make rs41558514(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356209
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs41558514
dbSNP (classic)rs41558514
ClinGenrs41558514
ebirs41558514
HLIrs41558514
Exacrs41558514
Gnomadrs41558514
Varsomers41558514
LitVarrs41558514
Maprs41558514
PheGenIrs41558514
Biobankrs41558514
1000 genomesrs41558514
hgdprs41558514
ensemblrs41558514
geneviewrs41558514
scholarrs41558514
googlers41558514
pharmgkbrs41558514
gwascentralrs41558514
openSNPrs41558514
23andMers41558514
SNPshotrs41558514
SNPdbers41558514
MSV3drs41558514
GWAS Ctlgrs41558514
Max Magnitude0
ClinVar
Risk rs41558514(A;A) rs41558514(T;T)
Alt rs41558514(A;A) rs41558514(T;T)
Reference Rs41558514(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323986G>A; NC_000006.11:g.31323986G>T
CLNSRC
CLNACC