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rs41561920

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41561920(C;G)
Make rs41561920(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356631
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41561920
ebirs41561920
HLIrs41561920
Exacrs41561920
Varsomers41561920
Maprs41561920
PheGenIrs41561920
hapmaprs41561920
1000 genomesrs41561920
hgdprs41561920
ensemblrs41561920
gopubmedrs41561920
geneviewrs41561920
scholarrs41561920
googlers41561920
pharmgkbrs41561920
gwascentralrs41561920
openSNPrs41561920
23andMers41561920
23andMe allrs41561920
SNP Nexus

SNPshotrs41561920
SNPdbers41561920
MSV3drs41561920
GWAS Ctlgrs41561920
Max Magnitude0
ClinVar
Risk rs41561920(G;G)
Alt rs41561920(G;G)
Reference rs41561920(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324408G>C
CLNSRC
CLNACC