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

rs41557417

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41557417(A;A)
Make rs41557417(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356543
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41557417
ebirs41557417
HLIrs41557417
Exacrs41557417
Varsomers41557417
Maprs41557417
PheGenIrs41557417
hapmaprs41557417
1000 genomesrs41557417
hgdprs41557417
ensemblrs41557417
gopubmedrs41557417
geneviewrs41557417
scholarrs41557417
googlers41557417
pharmgkbrs41557417
gwascentralrs41557417
openSNPrs41557417
23andMers41557417
23andMe allrs41557417
SNP Nexus

SNPshotrs41557417
SNPdbers41557417
MSV3drs41557417
GWAS Ctlgrs41557417
Max Magnitude0
ClinVar
Risk rs41557417(A;A)
Alt rs41557417(A;A)
Reference rs41557417(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324320G>T
CLNSRC
CLNACC