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

rs41555119

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41555119(-;-)
Make rs41555119(-;A)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355405
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs41555119
dbSNP (old)rs41555119
ClinGenrs41555119
ebirs41555119
HLIrs41555119
Exacrs41555119
Varsomers41555119
Maprs41555119
PheGenIrs41555119
Biobankrs41555119
1000 genomesrs41555119
hgdprs41555119
ensemblrs41555119
gopubmedrs41555119
geneviewrs41555119
scholarrs41555119
googlers41555119
pharmgkbrs41555119
gwascentralrs41555119
openSNPrs41555119
23andMers41555119
23andMe allrs41555119
SNP Nexus

SNPshotrs41555119
SNPdbers41555119
MSV3drs41555119
GWAS Ctlgrs41555119
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs41555119(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323182delT
CLNSRC
CLNACC