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rs41545020

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41545020(A;A)
Make rs41545020(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356830
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41545020
ebirs41545020
HLIrs41545020
Exacrs41545020
Varsomers41545020
Maprs41545020
PheGenIrs41545020
hapmaprs41545020
1000 genomesrs41545020
hgdprs41545020
ensemblrs41545020
gopubmedrs41545020
geneviewrs41545020
scholarrs41545020
googlers41545020
pharmgkbrs41545020
gwascentralrs41545020
openSNPrs41545020
23andMers41545020
23andMe allrs41545020
SNP Nexus

SNPshotrs41545020
SNPdbers41545020
MSV3drs41545020
GWAS Ctlgrs41545020
Max Magnitude0
ClinVar
Risk rs41545020(A,C,T;A,C,T)
Alt rs41545020(A,C,T;A,C,T)
Reference rs41545020(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324607C>A; NC_000006.11:g.31324607C>G; NC_000006.11:g.31324607C>T
CLNSRC
CLNACC