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rs41550715

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41550715(C;G)
Make rs41550715(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271215
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41550715
ebirs41550715
HLIrs41550715
Exacrs41550715
Varsomers41550715
Maprs41550715
PheGenIrs41550715
hapmaprs41550715
1000 genomesrs41550715
hgdprs41550715
ensemblrs41550715
gopubmedrs41550715
geneviewrs41550715
scholarrs41550715
googlers41550715
pharmgkbrs41550715
gwascentralrs41550715
openSNPrs41550715
23andMers41550715
23andMe allrs41550715
SNP Nexus

SNPshotrs41550715
SNPdbers41550715
MSV3drs41550715
GWAS Ctlgrs41550715
GMAF0.259
Max Magnitude0
ClinVar
Risk rs41550715(G,T;G,T)
Alt rs41550715(G,T;G,T)
Reference rs41550715(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238992G>A; NC_000006.11:g.31238992G>C
CLNSRC
CLNACC