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rs41550023

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41550023(A;A)
Make rs41550023(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271246
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41550023
ebirs41550023
HLIrs41550023
Exacrs41550023
Varsomers41550023
Maprs41550023
PheGenIrs41550023
hapmaprs41550023
1000 genomesrs41550023
hgdprs41550023
ensemblrs41550023
gopubmedrs41550023
geneviewrs41550023
scholarrs41550023
googlers41550023
pharmgkbrs41550023
gwascentralrs41550023
openSNPrs41550023
23andMers41550023
23andMe allrs41550023
SNP Nexus

SNPshotrs41550023
SNPdbers41550023
MSV3drs41550023
GWAS Ctlgrs41550023
Max Magnitude0
ClinVar
Risk rs41550023(A,T;A,T)
Alt rs41550023(A,T;A,T)
Reference rs41550023(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239023G>A; NC_000006.11:g.31239023G>T
CLNSRC
CLNACC