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rs41560619

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41560619(-;-)
Make rs41560619(-;T)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324757
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41560619
ebirs41560619
HLIrs41560619
Exacrs41560619
Varsomers41560619
Maprs41560619
PheGenIrs41560619
hapmaprs41560619
1000 genomesrs41560619
hgdprs41560619
ensemblrs41560619
gopubmedrs41560619
geneviewrs41560619
scholarrs41560619
googlers41560619
pharmgkbrs41560619
gwascentralrs41560619
openSNPrs41560619
23andMers41560619
23andMe allrs41560619
SNP Nexus

SNPshotrs41560619
SNPdbers41560619
MSV3drs41560619
GWAS Ctlgrs41560619
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41560619(;)
Alt rs41560619(;)
Reference rs41560619(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324757delA
CLNSRC
CLNACC