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rs41559915

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41559915(C;T)
Make rs41559915(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269498
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41559915
ebirs41559915
HLIrs41559915
Exacrs41559915
Varsomers41559915
Maprs41559915
PheGenIrs41559915
hapmaprs41559915
1000 genomesrs41559915
hgdprs41559915
ensemblrs41559915
gopubmedrs41559915
geneviewrs41559915
scholarrs41559915
googlers41559915
pharmgkbrs41559915
gwascentralrs41559915
openSNPrs41559915
23andMers41559915
23andMe allrs41559915
SNP Nexus

SNPshotrs41559915
SNPdbers41559915
MSV3drs41559915
GWAS Ctlgrs41559915
GMAF0.01515
Max Magnitude0
ClinVar
Risk rs41559915(T;T)
Alt rs41559915(T;T)
Reference rs41559915(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237275G>A
CLNSRC
CLNACC