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rs41563012

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41563012(A;A)
Make rs41563012(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356844
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41563012
ebirs41563012
HLIrs41563012
Exacrs41563012
Varsomers41563012
Maprs41563012
PheGenIrs41563012
hapmaprs41563012
1000 genomesrs41563012
hgdprs41563012
ensemblrs41563012
gopubmedrs41563012
geneviewrs41563012
scholarrs41563012
googlers41563012
pharmgkbrs41563012
gwascentralrs41563012
openSNPrs41563012
23andMers41563012
23andMe allrs41563012
SNP Nexus

SNPshotrs41563012
SNPdbers41563012
MSV3drs41563012
GWAS Ctlgrs41563012
Max Magnitude0
ClinVar
Risk rs41563012(A;A)
Alt rs41563012(A;A)
Reference rs41563012(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324621C>T
CLNSRC
CLNACC