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rs41550819

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41550819(C;C)
Make rs41550819(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270939
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41550819
ebirs41550819
HLIrs41550819
Exacrs41550819
Varsomers41550819
Maprs41550819
PheGenIrs41550819
hapmaprs41550819
1000 genomesrs41550819
hgdprs41550819
ensemblrs41550819
gopubmedrs41550819
geneviewrs41550819
scholarrs41550819
googlers41550819
pharmgkbrs41550819
gwascentralrs41550819
openSNPrs41550819
23andMers41550819
23andMe allrs41550819
SNP Nexus

SNPshotrs41550819
SNPdbers41550819
MSV3drs41550819
GWAS Ctlgrs41550819
GMAF0.03168
Max Magnitude0
ClinVar
Risk rs41550819(C;C)
Alt rs41550819(C;C)
Reference rs41550819(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238716A>G
CLNSRC
CLNACC