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rs41549412

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41549412(A;A)
Make rs41549412(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356172
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41549412
ebirs41549412
HLIrs41549412
Exacrs41549412
Varsomers41549412
Maprs41549412
PheGenIrs41549412
hapmaprs41549412
1000 genomesrs41549412
hgdprs41549412
ensemblrs41549412
gopubmedrs41549412
geneviewrs41549412
scholarrs41549412
googlers41549412
pharmgkbrs41549412
gwascentralrs41549412
openSNPrs41549412
23andMers41549412
23andMe allrs41549412
SNP Nexus

SNPshotrs41549412
SNPdbers41549412
MSV3drs41549412
GWAS Ctlgrs41549412
Max Magnitude0
ClinVar
Risk rs41549412(A;A)
Alt rs41549412(A;A)
Reference rs41549412(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323949C>T
CLNSRC
CLNACC