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rs41552417

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41552417(A;A)
Make rs41552417(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271097
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41552417
ebirs41552417
HLIrs41552417
Exacrs41552417
Varsomers41552417
Maprs41552417
PheGenIrs41552417
hapmaprs41552417
1000 genomesrs41552417
hgdprs41552417
ensemblrs41552417
gopubmedrs41552417
geneviewrs41552417
scholarrs41552417
googlers41552417
pharmgkbrs41552417
gwascentralrs41552417
openSNPrs41552417
23andMers41552417
23andMe allrs41552417
SNP Nexus

SNPshotrs41552417
SNPdbers41552417
MSV3drs41552417
GWAS Ctlgrs41552417
Max Magnitude0
ClinVar
Risk rs41552417(A,C,T;A,C,T)
Alt rs41552417(A,C,T;A,C,T)
Reference rs41552417(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238874C>A; NC_000006.11:g.31238874C>G; NC_000006.11:g.31238874C>T
CLNSRC
CLNACC