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rs41549513

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41549513(A;A)
Make rs41549513(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356716
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs41549513
dbSNP (old)rs41549513
ClinGenrs41549513
ebirs41549513
HLIrs41549513
Exacrs41549513
Gnomadrs41549513
Varsomers41549513
Maprs41549513
PheGenIrs41549513
Biobankrs41549513
1000 genomesrs41549513
hgdprs41549513
ensemblrs41549513
gopubmedrs41549513
geneviewrs41549513
scholarrs41549513
googlers41549513
pharmgkbrs41549513
gwascentralrs41549513
openSNPrs41549513
23andMers41549513
23andMe allrs41549513
SNP Nexus

SNPshotrs41549513
SNPdbers41549513
MSV3drs41549513
GWAS Ctlgrs41549513
Max Magnitude0
ClinVar
Risk rs41549513(A;A) rs41549513(C;C)
Alt rs41549513(A;A) rs41549513(C;C)
Reference Rs41549513(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324493C>G; NC_000006.11:g.31324493C>T
CLNSRC
CLNACC