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rs41542612

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41542612(C;T)
Make rs41542612(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271225
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41542612
ebirs41542612
HLIrs41542612
Exacrs41542612
Varsomers41542612
Maprs41542612
PheGenIrs41542612
hapmaprs41542612
1000 genomesrs41542612
hgdprs41542612
ensemblrs41542612
gopubmedrs41542612
geneviewrs41542612
scholarrs41542612
googlers41542612
pharmgkbrs41542612
gwascentralrs41542612
openSNPrs41542612
23andMers41542612
23andMe allrs41542612
SNP Nexus

SNPshotrs41542612
SNPdbers41542612
MSV3drs41542612
GWAS Ctlgrs41542612
Max Magnitude0
ClinVar
Risk rs41542612(T;T)
Alt rs41542612(T;T)
Reference rs41542612(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239002G>A
CLNSRC
CLNACC