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rs41544813

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41544813(C;G)
Make rs41544813(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271520
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41544813
ebirs41544813
HLIrs41544813
Exacrs41544813
Varsomers41544813
Maprs41544813
PheGenIrs41544813
hapmaprs41544813
1000 genomesrs41544813
hgdprs41544813
ensemblrs41544813
gopubmedrs41544813
geneviewrs41544813
scholarrs41544813
googlers41544813
pharmgkbrs41544813
gwascentralrs41544813
openSNPrs41544813
23andMers41544813
23andMe allrs41544813
SNP Nexus

SNPshotrs41544813
SNPdbers41544813
MSV3drs41544813
GWAS Ctlgrs41544813
GMAF0.03673
Max Magnitude0
ClinVar
Risk rs41544813(G;G)
Alt rs41544813(G;G)
Reference rs41544813(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239297G>C
CLNSRC
CLNACC