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rs41560417

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41560417(G;G)
Make rs41560417(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355331
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41560417
ebirs41560417
HLIrs41560417
Exacrs41560417
Varsomers41560417
Maprs41560417
PheGenIrs41560417
hapmaprs41560417
1000 genomesrs41560417
hgdprs41560417
ensemblrs41560417
gopubmedrs41560417
geneviewrs41560417
scholarrs41560417
googlers41560417
pharmgkbrs41560417
gwascentralrs41560417
openSNPrs41560417
23andMers41560417
23andMe allrs41560417
SNP Nexus

SNPshotrs41560417
SNPdbers41560417
MSV3drs41560417
GWAS Ctlgrs41560417
Max Magnitude0
ClinVar
Risk rs41560417(G;G)
Alt rs41560417(G;G)
Reference rs41560417(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323108A>C
CLNSRC
CLNACC