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rs41561814

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41561814(A;A)
Make rs41561814(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356350
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41561814
ebirs41561814
HLIrs41561814
Exacrs41561814
Varsomers41561814
Maprs41561814
PheGenIrs41561814
hapmaprs41561814
1000 genomesrs41561814
hgdprs41561814
ensemblrs41561814
gopubmedrs41561814
geneviewrs41561814
scholarrs41561814
googlers41561814
pharmgkbrs41561814
gwascentralrs41561814
openSNPrs41561814
23andMers41561814
23andMe allrs41561814
SNP Nexus

SNPshotrs41561814
SNPdbers41561814
MSV3drs41561814
GWAS Ctlgrs41561814
Max Magnitude0
ClinVar
Risk rs41561814(A;A)
Alt rs41561814(A;A)
Reference rs41561814(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324127C>T
CLNSRC
CLNACC