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rs41561913

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41561913(C;T)
Make rs41561913(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271016
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41561913
ebirs41561913
HLIrs41561913
Exacrs41561913
Varsomers41561913
Maprs41561913
PheGenIrs41561913
hapmaprs41561913
1000 genomesrs41561913
hgdprs41561913
ensemblrs41561913
gopubmedrs41561913
geneviewrs41561913
scholarrs41561913
googlers41561913
pharmgkbrs41561913
gwascentralrs41561913
openSNPrs41561913
23andMers41561913
23andMe allrs41561913
SNP Nexus

SNPshotrs41561913
SNPdbers41561913
MSV3drs41561913
GWAS Ctlgrs41561913
GMAF0.02893
Max Magnitude0
ClinVar
Risk rs41561913(T;T)
Alt rs41561913(T;T)
Reference rs41561913(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238793G>A
CLNSRC
CLNACC