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rs61760866

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61760866(-;-)
Make rs61760866(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position29910739
GeneHLA-A
is asnp
is mentioned by
dbSNPrs61760866
ebirs61760866
HLIrs61760866
Exacrs61760866
Varsomers61760866
Maprs61760866
PheGenIrs61760866
hapmaprs61760866
1000 genomesrs61760866
hgdprs61760866
ensemblrs61760866
gopubmedrs61760866
geneviewrs61760866
scholarrs61760866
googlers61760866
pharmgkbrs61760866
gwascentralrs61760866
openSNPrs61760866
23andMers61760866
23andMe allrs61760866
SNP Nexus

SNPshotrs61760866
SNPdbers61760866
MSV3drs61760866
GWAS Ctlgrs61760866
StatusDeleted
Max Magnitude0
ClinVar
Risk rs61760866(;)
Alt rs61760866(;)
Reference rs61760866(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910739delC
CLNSRC
CLNACC