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rs41552718

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41552718(C;C)
Make rs41552718(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269482
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41552718
ebirs41552718
HLIrs41552718
Exacrs41552718
Varsomers41552718
Maprs41552718
PheGenIrs41552718
hapmaprs41552718
1000 genomesrs41552718
hgdprs41552718
ensemblrs41552718
gopubmedrs41552718
geneviewrs41552718
scholarrs41552718
googlers41552718
pharmgkbrs41552718
gwascentralrs41552718
openSNPrs41552718
23andMers41552718
23andMe allrs41552718
SNP Nexus

SNPshotrs41552718
SNPdbers41552718
MSV3drs41552718
GWAS Ctlgrs41552718
Max Magnitude0
ClinVar
Risk rs41552718(C;C)
Alt rs41552718(C;C)
Reference rs41552718(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237259C>G
CLNSRC
CLNACC