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rs41546212

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41546212(-;-)
Make rs41546212(-;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356381
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41546212
ebirs41546212
HLIrs41546212
Exacrs41546212
Varsomers41546212
Maprs41546212
PheGenIrs41546212
hapmaprs41546212
1000 genomesrs41546212
hgdprs41546212
ensemblrs41546212
gopubmedrs41546212
geneviewrs41546212
scholarrs41546212
googlers41546212
pharmgkbrs41546212
gwascentralrs41546212
openSNPrs41546212
23andMers41546212
23andMe allrs41546212
SNP Nexus

SNPshotrs41546212
SNPdbers41546212
MSV3drs41546212
GWAS Ctlgrs41546212
Max Magnitude0
ClinVar
Risk rs41546212(;)
Alt rs41546212(;)
Reference rs41546212(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324158delG
CLNSRC
CLNACC