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rs41551014

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41551014(C;C)
Make rs41551014(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355351
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41551014
ebirs41551014
HLIrs41551014
Exacrs41551014
Varsomers41551014
Maprs41551014
PheGenIrs41551014
hapmaprs41551014
1000 genomesrs41551014
hgdprs41551014
ensemblrs41551014
gopubmedrs41551014
geneviewrs41551014
scholarrs41551014
googlers41551014
pharmgkbrs41551014
gwascentralrs41551014
openSNPrs41551014
23andMers41551014
23andMe allrs41551014
SNP Nexus

SNPshotrs41551014
SNPdbers41551014
MSV3drs41551014
GWAS Ctlgrs41551014
Max Magnitude0
ClinVar
Risk rs41551014(C;C)
Alt rs41551014(C;C)
Reference rs41551014(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323128A>G
CLNSRC
CLNACC