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rs41553719

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41553719(G;G)
Make rs41553719(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271274
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41553719
ebirs41553719
HLIrs41553719
Exacrs41553719
Varsomers41553719
Maprs41553719
PheGenIrs41553719
hapmaprs41553719
1000 genomesrs41553719
hgdprs41553719
ensemblrs41553719
gopubmedrs41553719
geneviewrs41553719
scholarrs41553719
googlers41553719
pharmgkbrs41553719
gwascentralrs41553719
openSNPrs41553719
23andMers41553719
23andMe allrs41553719
SNP Nexus

SNPshotrs41553719
SNPdbers41553719
MSV3drs41553719
GWAS Ctlgrs41553719
Max Magnitude0
ClinVar
Risk rs41553719(G;G)
Alt rs41553719(G;G)
Reference rs41553719(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239051A>C
CLNSRC
CLNACC