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

rs41544719

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41544719(A;A)
Make rs41544719(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356558
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41544719
ebirs41544719
HLIrs41544719
Exacrs41544719
Varsomers41544719
Maprs41544719
PheGenIrs41544719
hapmaprs41544719
1000 genomesrs41544719
hgdprs41544719
ensemblrs41544719
gopubmedrs41544719
geneviewrs41544719
scholarrs41544719
googlers41544719
pharmgkbrs41544719
gwascentralrs41544719
openSNPrs41544719
23andMers41544719
23andMe allrs41544719
SNP Nexus

SNPshotrs41544719
SNPdbers41544719
MSV3drs41544719
GWAS Ctlgrs41544719
Max Magnitude0
ClinVar
Risk rs41544719(A;A)
Alt rs41544719(A;A)
Reference rs41544719(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324335G>T
CLNSRC
CLNACC