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rs41560220

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41560220(A;A)
Make rs41560220(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356098
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41560220
ebirs41560220
HLIrs41560220
Exacrs41560220
Varsomers41560220
Maprs41560220
PheGenIrs41560220
hapmaprs41560220
1000 genomesrs41560220
hgdprs41560220
ensemblrs41560220
gopubmedrs41560220
geneviewrs41560220
scholarrs41560220
googlers41560220
pharmgkbrs41560220
gwascentralrs41560220
openSNPrs41560220
23andMers41560220
23andMe allrs41560220
SNP Nexus

SNPshotrs41560220
SNPdbers41560220
MSV3drs41560220
GWAS Ctlgrs41560220
GMAF0.07208
Max Magnitude0
ClinVar
Risk rs41560220(A;A)
Alt rs41560220(A;A)
Reference rs41560220(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323875C>T
CLNSRC
CLNACC