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rs41557820

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41557820(A;A)
Make rs41557820(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356222
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41557820
ebirs41557820
HLIrs41557820
Exacrs41557820
Varsomers41557820
Maprs41557820
PheGenIrs41557820
hapmaprs41557820
1000 genomesrs41557820
hgdprs41557820
ensemblrs41557820
gopubmedrs41557820
geneviewrs41557820
scholarrs41557820
googlers41557820
pharmgkbrs41557820
gwascentralrs41557820
openSNPrs41557820
23andMers41557820
23andMe allrs41557820
SNP Nexus

SNPshotrs41557820
SNPdbers41557820
MSV3drs41557820
GWAS Ctlgrs41557820
Max Magnitude0
ClinVar
Risk rs41557820(A,G,T;A,G,T)
Alt rs41557820(A,G,T;A,G,T)
Reference rs41557820(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323999G>A; NC_000006.11:g.31323999G>C; NC_000006.11:g.31323999G>T
CLNSRC
CLNACC