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rs41558820

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41558820(A;A)
Make rs41558820(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271615
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41558820
ebirs41558820
HLIrs41558820
Exacrs41558820
Varsomers41558820
Maprs41558820
PheGenIrs41558820
hapmaprs41558820
1000 genomesrs41558820
hgdprs41558820
ensemblrs41558820
gopubmedrs41558820
geneviewrs41558820
scholarrs41558820
googlers41558820
pharmgkbrs41558820
gwascentralrs41558820
openSNPrs41558820
23andMers41558820
23andMe allrs41558820
SNP Nexus

SNPshotrs41558820
SNPdbers41558820
MSV3drs41558820
GWAS Ctlgrs41558820
Max Magnitude0
ClinVar
Risk rs41558820(A,T;A,T)
Alt rs41558820(A,T;A,T)
Reference rs41558820(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239392G>A; NC_000006.11:g.31239392G>T
CLNSRC
CLNACC