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rs41546913

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41546913(A;A)
Make rs41546913(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271336
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41546913
ebirs41546913
HLIrs41546913
Exacrs41546913
Varsomers41546913
Maprs41546913
PheGenIrs41546913
hapmaprs41546913
1000 genomesrs41546913
hgdprs41546913
ensemblrs41546913
gopubmedrs41546913
geneviewrs41546913
scholarrs41546913
googlers41546913
pharmgkbrs41546913
gwascentralrs41546913
openSNPrs41546913
23andMers41546913
23andMe allrs41546913
SNP Nexus

SNPshotrs41546913
SNPdbers41546913
MSV3drs41546913
GWAS Ctlgrs41546913
Max Magnitude0
ClinVar
Risk rs41546913(A,C,G;A,C,G)
Alt rs41546913(A,C,G;A,C,G)
Reference rs41546913(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239113A>G; NC_000006.11:g.31239113A>T
CLNSRC
CLNACC