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rs41540616

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41540616(-;-)
Make rs41540616(-;T)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324755
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41540616
ebirs41540616
HLIrs41540616
Exacrs41540616
Varsomers41540616
Maprs41540616
PheGenIrs41540616
hapmaprs41540616
1000 genomesrs41540616
hgdprs41540616
ensemblrs41540616
gopubmedrs41540616
geneviewrs41540616
scholarrs41540616
googlers41540616
pharmgkbrs41540616
gwascentralrs41540616
openSNPrs41540616
23andMers41540616
23andMe allrs41540616
SNP Nexus

SNPshotrs41540616
SNPdbers41540616
MSV3drs41540616
GWAS Ctlgrs41540616
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41540616(;)
Alt rs41540616(;)
Reference rs41540616(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324755delA
CLNSRC
CLNACC