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rs41559713

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41559713(A;G)
Make rs41559713(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271641
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41559713
ebirs41559713
HLIrs41559713
Exacrs41559713
Varsomers41559713
Maprs41559713
PheGenIrs41559713
hapmaprs41559713
1000 genomesrs41559713
hgdprs41559713
ensemblrs41559713
gopubmedrs41559713
geneviewrs41559713
scholarrs41559713
googlers41559713
pharmgkbrs41559713
gwascentralrs41559713
openSNPrs41559713
23andMers41559713
23andMe allrs41559713
SNP Nexus

SNPshotrs41559713
SNPdbers41559713
MSV3drs41559713
GWAS Ctlgrs41559713
Max Magnitude0
ClinVar
Risk rs41559713(G,T;G,T)
Alt rs41559713(G,T;G,T)
Reference rs41559713(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239418T>A; NC_000006.11:g.31239418T>C
CLNSRC
CLNACC