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rs41562313

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41562313(C;C)
Make rs41562313(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271281
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41562313
ebirs41562313
HLIrs41562313
Exacrs41562313
Varsomers41562313
Maprs41562313
PheGenIrs41562313
hapmaprs41562313
1000 genomesrs41562313
hgdprs41562313
ensemblrs41562313
gopubmedrs41562313
geneviewrs41562313
scholarrs41562313
googlers41562313
pharmgkbrs41562313
gwascentralrs41562313
openSNPrs41562313
23andMers41562313
23andMe allrs41562313
SNP Nexus

SNPshotrs41562313
SNPdbers41562313
MSV3drs41562313
GWAS Ctlgrs41562313
Max Magnitude0
ClinVar
Risk rs41562313(C,G;C,G)
Alt rs41562313(C,G;C,G)
Reference rs41562313(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239058A>C; NC_000006.11:g.31239058A>G
CLNSRC
CLNACC