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rs41551113

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41551113(A;A)
Make rs41551113(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355319
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41551113
ebirs41551113
HLIrs41551113
Exacrs41551113
Varsomers41551113
Maprs41551113
PheGenIrs41551113
hapmaprs41551113
1000 genomesrs41551113
hgdprs41551113
ensemblrs41551113
gopubmedrs41551113
geneviewrs41551113
scholarrs41551113
googlers41551113
pharmgkbrs41551113
gwascentralrs41551113
openSNPrs41551113
23andMers41551113
23andMe allrs41551113
SNP Nexus

SNPshotrs41551113
SNPdbers41551113
MSV3drs41551113
GWAS Ctlgrs41551113
Max Magnitude0
ClinVar
Risk rs41551113(A;A)
Alt rs41551113(A;A)
Reference rs41551113(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323096C>T
CLNSRC
CLNACC