Have questions? Visit https://www.reddit.com/r/SNPedia

rs41557013

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41557013(C;T)
Make rs41557013(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355457
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41557013
ebirs41557013
HLIrs41557013
Exacrs41557013
Varsomers41557013
Maprs41557013
PheGenIrs41557013
hapmaprs41557013
1000 genomesrs41557013
hgdprs41557013
ensemblrs41557013
gopubmedrs41557013
geneviewrs41557013
scholarrs41557013
googlers41557013
pharmgkbrs41557013
gwascentralrs41557013
openSNPrs41557013
23andMers41557013
23andMe allrs41557013
SNP Nexus

SNPshotrs41557013
SNPdbers41557013
MSV3drs41557013
GWAS Ctlgrs41557013
Max Magnitude0
ClinVar
Risk rs41557013(T;T)
Alt rs41557013(T;T)
Reference rs41557013(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323234G>A
CLNSRC
CLNACC