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rs41546813

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41546813(A;A)
Make rs41546813(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271586
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41546813
ebirs41546813
HLIrs41546813
Exacrs41546813
Varsomers41546813
Maprs41546813
PheGenIrs41546813
hapmaprs41546813
1000 genomesrs41546813
hgdprs41546813
ensemblrs41546813
gopubmedrs41546813
geneviewrs41546813
scholarrs41546813
googlers41546813
pharmgkbrs41546813
gwascentralrs41546813
openSNPrs41546813
23andMers41546813
23andMe allrs41546813
SNP Nexus

SNPshotrs41546813
SNPdbers41546813
MSV3drs41546813
GWAS Ctlgrs41546813
GMAF0.0225
Max Magnitude0
ClinVar
Risk rs41546813(A;A)
Alt rs41546813(A;A)
Reference rs41546813(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239363C>T
CLNSRC
CLNACC