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rs41563413

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41563413(G;G)
Make rs41563413(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271346
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41563413
ebirs41563413
HLIrs41563413
Exacrs41563413
Varsomers41563413
Maprs41563413
PheGenIrs41563413
hapmaprs41563413
1000 genomesrs41563413
hgdprs41563413
ensemblrs41563413
gopubmedrs41563413
geneviewrs41563413
scholarrs41563413
googlers41563413
pharmgkbrs41563413
gwascentralrs41563413
openSNPrs41563413
23andMers41563413
23andMe allrs41563413
SNP Nexus

SNPshotrs41563413
SNPdbers41563413
MSV3drs41563413
GWAS Ctlgrs41563413
Max Magnitude0
ClinVar
Risk rs41563413(G;G)
Alt rs41563413(G;G)
Reference rs41563413(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239123A>C
CLNSRC
CLNACC