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rs41556912

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41556912(-;-)
Make rs41556912(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position29911059
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41556912
ebirs41556912
HLIrs41556912
Exacrs41556912
Varsomers41556912
Maprs41556912
PheGenIrs41556912
hapmaprs41556912
1000 genomesrs41556912
hgdprs41556912
ensemblrs41556912
gopubmedrs41556912
geneviewrs41556912
scholarrs41556912
googlers41556912
pharmgkbrs41556912
gwascentralrs41556912
openSNPrs41556912
23andMers41556912
23andMe allrs41556912
SNP Nexus

SNPshotrs41556912
SNPdbers41556912
MSV3drs41556912
GWAS Ctlgrs41556912
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41556912(;)
Alt rs41556912(;)
Reference rs41556912(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911059delC
CLNSRC
CLNACC