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rs41550619

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41550619(A;A)
Make rs41550619(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271643
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41550619
ebirs41550619
HLIrs41550619
Exacrs41550619
Varsomers41550619
Maprs41550619
PheGenIrs41550619
hapmaprs41550619
1000 genomesrs41550619
hgdprs41550619
ensemblrs41550619
gopubmedrs41550619
geneviewrs41550619
scholarrs41550619
googlers41550619
pharmgkbrs41550619
gwascentralrs41550619
openSNPrs41550619
23andMers41550619
23andMe allrs41550619
SNP Nexus

SNPshotrs41550619
SNPdbers41550619
MSV3drs41550619
GWAS Ctlgrs41550619
Max Magnitude0
ClinVar
Risk rs41550619(A;A)
Alt rs41550619(A;A)
Reference rs41550619(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239420A>T
CLNSRC
CLNACC