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rs41555116

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41555116(-;-)
Make rs41555116(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position29910323
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41555116
ebirs41555116
HLIrs41555116
Exacrs41555116
Varsomers41555116
Maprs41555116
PheGenIrs41555116
hapmaprs41555116
1000 genomesrs41555116
hgdprs41555116
ensemblrs41555116
gopubmedrs41555116
geneviewrs41555116
scholarrs41555116
googlers41555116
pharmgkbrs41555116
gwascentralrs41555116
openSNPrs41555116
23andMers41555116
23andMe allrs41555116
SNP Nexus

SNPshotrs41555116
SNPdbers41555116
MSV3drs41555116
GWAS Ctlgrs41555116
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41555116(;)
Alt rs41555116(;)
Reference rs41555116(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910323delC
CLNSRC
CLNACC