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rs61760863

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs61760863(-;-)
Make rs61760863(-;T)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position29910732
GeneHLA-A
is asnp
is mentioned by
dbSNPrs61760863
ebirs61760863
HLIrs61760863
Exacrs61760863
Varsomers61760863
Maprs61760863
PheGenIrs61760863
hapmaprs61760863
1000 genomesrs61760863
hgdprs61760863
ensemblrs61760863
gopubmedrs61760863
geneviewrs61760863
scholarrs61760863
googlers61760863
pharmgkbrs61760863
gwascentralrs61760863
openSNPrs61760863
23andMers61760863
23andMe allrs61760863
SNP Nexus

SNPshotrs61760863
SNPdbers61760863
MSV3drs61760863
GWAS Ctlgrs61760863
StatusDeleted
Max Magnitude0
ClinVar
Risk rs61760863(;)
Alt rs61760863(;)
Reference rs61760863(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910732delT
CLNSRC
CLNACC