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rs41560817

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41560817(A;A)
Make rs41560817(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356372
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41560817
ebirs41560817
HLIrs41560817
Exacrs41560817
Varsomers41560817
Maprs41560817
PheGenIrs41560817
hapmaprs41560817
1000 genomesrs41560817
hgdprs41560817
ensemblrs41560817
gopubmedrs41560817
geneviewrs41560817
scholarrs41560817
googlers41560817
pharmgkbrs41560817
gwascentralrs41560817
openSNPrs41560817
23andMers41560817
23andMe allrs41560817
SNP Nexus

SNPshotrs41560817
SNPdbers41560817
MSV3drs41560817
GWAS Ctlgrs41560817
Max Magnitude0
ClinVar
Risk rs41560817(A,G,T;A,G,T)
Alt rs41560817(A,G,T;A,G,T)
Reference rs41560817(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324149G>A; NC_000006.11:g.31324149G>C; NC_000006.11:g.31324149G>T
CLNSRC
CLNACC