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rs41548020

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41548020(-;-)
Make rs41548020(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324583
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41548020
ebirs41548020
HLIrs41548020
Exacrs41548020
Varsomers41548020
Maprs41548020
PheGenIrs41548020
hapmaprs41548020
1000 genomesrs41548020
hgdprs41548020
ensemblrs41548020
gopubmedrs41548020
geneviewrs41548020
scholarrs41548020
googlers41548020
pharmgkbrs41548020
gwascentralrs41548020
openSNPrs41548020
23andMers41548020
23andMe allrs41548020
SNP Nexus

SNPshotrs41548020
SNPdbers41548020
MSV3drs41548020
GWAS Ctlgrs41548020
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41548020(;)
Alt rs41548020(;)
Reference rs41548020(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324583delC
CLNSRC
CLNACC