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rs41546713

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41546713(G;G)
Make rs41546713(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270224
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41546713
ebirs41546713
HLIrs41546713
Exacrs41546713
Varsomers41546713
Maprs41546713
PheGenIrs41546713
hapmaprs41546713
1000 genomesrs41546713
hgdprs41546713
ensemblrs41546713
gopubmedrs41546713
geneviewrs41546713
scholarrs41546713
googlers41546713
pharmgkbrs41546713
gwascentralrs41546713
openSNPrs41546713
23andMers41546713
23andMe allrs41546713
SNP Nexus

SNPshotrs41546713
SNPdbers41546713
MSV3drs41546713
GWAS Ctlgrs41546713
Max Magnitude0
ClinVar
Risk rs41546713(G;G)
Alt rs41546713(G;G)
Reference rs41546713(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238001A>C
CLNSRC
CLNACC