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rs41557213

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41557213(A;A)
Make rs41557213(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357042
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41557213
ebirs41557213
HLIrs41557213
Exacrs41557213
Varsomers41557213
Maprs41557213
PheGenIrs41557213
hapmaprs41557213
1000 genomesrs41557213
hgdprs41557213
ensemblrs41557213
gopubmedrs41557213
geneviewrs41557213
scholarrs41557213
googlers41557213
pharmgkbrs41557213
gwascentralrs41557213
openSNPrs41557213
23andMers41557213
23andMe allrs41557213
SNP Nexus

SNPshotrs41557213
SNPdbers41557213
MSV3drs41557213
GWAS Ctlgrs41557213
GMAF0.03076
Max Magnitude0
ClinVar
Risk rs41557213(A;A)
Alt rs41557213(A;A)
Reference rs41557213(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324819C>T
CLNSRC
CLNACC