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rs41560517

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41560517(A;A)
Make rs41560517(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356306
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41560517
ebirs41560517
HLIrs41560517
Exacrs41560517
Varsomers41560517
Maprs41560517
PheGenIrs41560517
hapmaprs41560517
1000 genomesrs41560517
hgdprs41560517
ensemblrs41560517
gopubmedrs41560517
geneviewrs41560517
scholarrs41560517
googlers41560517
pharmgkbrs41560517
gwascentralrs41560517
openSNPrs41560517
23andMers41560517
23andMe allrs41560517
SNP Nexus

SNPshotrs41560517
SNPdbers41560517
MSV3drs41560517
GWAS Ctlgrs41560517
Max Magnitude0
ClinVar
Risk rs41560517(A,C,T;A,C,T)
Alt rs41560517(A,C,T;A,C,T)
Reference rs41560517(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324083C>A; NC_000006.11:g.31324083C>G; NC_000006.11:g.31324083C>T
CLNSRC
CLNACC