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rs41549713

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41549713(-;-)
Make rs41549713(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324579
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41549713
ebirs41549713
HLIrs41549713
Exacrs41549713
Varsomers41549713
Maprs41549713
PheGenIrs41549713
hapmaprs41549713
1000 genomesrs41549713
hgdprs41549713
ensemblrs41549713
gopubmedrs41549713
geneviewrs41549713
scholarrs41549713
googlers41549713
pharmgkbrs41549713
gwascentralrs41549713
openSNPrs41549713
23andMers41549713
23andMe allrs41549713
SNP Nexus

SNPshotrs41549713
SNPdbers41549713
MSV3drs41549713
GWAS Ctlgrs41549713
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41549713(;)
Alt rs41549713(;)
Reference rs41549713(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324579delC
CLNSRC
CLNACC