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rs41540612

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41540612(-;-)
Make rs41540612(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324088
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41540612
ebirs41540612
HLIrs41540612
Exacrs41540612
Varsomers41540612
Maprs41540612
PheGenIrs41540612
hapmaprs41540612
1000 genomesrs41540612
hgdprs41540612
ensemblrs41540612
gopubmedrs41540612
geneviewrs41540612
scholarrs41540612
googlers41540612
pharmgkbrs41540612
gwascentralrs41540612
openSNPrs41540612
23andMers41540612
23andMe allrs41540612
SNP Nexus

SNPshotrs41540612
SNPdbers41540612
MSV3drs41540612
GWAS Ctlgrs41540612
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41540612(;)
Alt rs41540612(;)
Reference rs41540612(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324088delC
CLNSRC
CLNACC