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rs41558319

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41558319(-;-)
Make rs41558319(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position29911076
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41558319
ebirs41558319
HLIrs41558319
Exacrs41558319
Varsomers41558319
Maprs41558319
PheGenIrs41558319
hapmaprs41558319
1000 genomesrs41558319
hgdprs41558319
ensemblrs41558319
gopubmedrs41558319
geneviewrs41558319
scholarrs41558319
googlers41558319
pharmgkbrs41558319
gwascentralrs41558319
openSNPrs41558319
23andMers41558319
23andMe allrs41558319
SNP Nexus

SNPshotrs41558319
SNPdbers41558319
MSV3drs41558319
GWAS Ctlgrs41558319
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41558319(;)
Alt rs41558319(;)
Reference rs41558319(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911076delC
CLNSRC
CLNACC