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rs41543218

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41543218(G;T)
Make rs41543218(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271347
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41543218
ebirs41543218
HLIrs41543218
Exacrs41543218
Varsomers41543218
Maprs41543218
PheGenIrs41543218
hapmaprs41543218
1000 genomesrs41543218
hgdprs41543218
ensemblrs41543218
gopubmedrs41543218
geneviewrs41543218
scholarrs41543218
googlers41543218
pharmgkbrs41543218
gwascentralrs41543218
openSNPrs41543218
23andMers41543218
23andMe allrs41543218
SNP Nexus

SNPshotrs41543218
SNPdbers41543218
MSV3drs41543218
GWAS Ctlgrs41543218
Max Magnitude0
ClinVar
Risk rs41543218(T;T)
Alt rs41543218(T;T)
Reference rs41543218(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239124C>A
CLNSRC
CLNACC