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rs61760867

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61760867(-;-)
Make rs61760867(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position29910740
GeneHLA-A
is asnp
is mentioned by
dbSNPrs61760867
ebirs61760867
HLIrs61760867
Exacrs61760867
Varsomers61760867
Maprs61760867
PheGenIrs61760867
hapmaprs61760867
1000 genomesrs61760867
hgdprs61760867
ensemblrs61760867
gopubmedrs61760867
geneviewrs61760867
scholarrs61760867
googlers61760867
pharmgkbrs61760867
gwascentralrs61760867
openSNPrs61760867
23andMers61760867
23andMe allrs61760867
SNP Nexus

SNPshotrs61760867
SNPdbers61760867
MSV3drs61760867
GWAS Ctlgrs61760867
StatusDeleted
Max Magnitude0
ClinVar
Risk rs61760867(;)
Alt rs61760867(;)
Reference rs61760867(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910740delC
CLNSRC
CLNACC