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rs41554721

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41554721(C;G)
Make rs41554721(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355072
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41554721
ebirs41554721
HLIrs41554721
Exacrs41554721
Varsomers41554721
Maprs41554721
PheGenIrs41554721
hapmaprs41554721
1000 genomesrs41554721
hgdprs41554721
ensemblrs41554721
gopubmedrs41554721
geneviewrs41554721
scholarrs41554721
googlers41554721
pharmgkbrs41554721
gwascentralrs41554721
openSNPrs41554721
23andMers41554721
23andMe allrs41554721
SNP Nexus

SNPshotrs41554721
SNPdbers41554721
MSV3drs41554721
GWAS Ctlgrs41554721
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs41554721(G;G)
Alt rs41554721(G;G)
Reference rs41554721(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322849G>C
CLNSRC
CLNACC