Have questions? Visit https://www.reddit.com/r/SNPedia

rs41546015

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41546015(A;A)
Make rs41546015(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356303
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41546015
ebirs41546015
HLIrs41546015
Exacrs41546015
Varsomers41546015
Maprs41546015
PheGenIrs41546015
hapmaprs41546015
1000 genomesrs41546015
hgdprs41546015
ensemblrs41546015
gopubmedrs41546015
geneviewrs41546015
scholarrs41546015
googlers41546015
pharmgkbrs41546015
gwascentralrs41546015
openSNPrs41546015
23andMers41546015
23andMe allrs41546015
SNP Nexus

SNPshotrs41546015
SNPdbers41546015
MSV3drs41546015
GWAS Ctlgrs41546015
Max Magnitude0
ClinVar
Risk rs41546015(A,G;A,G)
Alt rs41546015(A,G;A,G)
Reference rs41546015(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324080G>C; NC_000006.11:g.31324080G>T
CLNSRC
CLNACC