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rs61760913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61760913(-;-)
Make rs61760913(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position29910746
GeneHLA-A
is asnp
is mentioned by
dbSNPrs61760913
dbSNP (classic)rs61760913
ClinGenrs61760913
ebirs61760913
HLIrs61760913
Exacrs61760913
Gnomadrs61760913
Varsomers61760913
LitVarrs61760913
Maprs61760913
PheGenIrs61760913
Biobankrs61760913
1000 genomesrs61760913
hgdprs61760913
ensemblrs61760913
geneviewrs61760913
scholarrs61760913
googlers61760913
pharmgkbrs61760913
gwascentralrs61760913
openSNPrs61760913
23andMers61760913
SNPshotrs61760913
SNPdbers61760913
MSV3drs61760913
GWAS Ctlgrs61760913
StatusDeleted
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs61760913(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910746delC
CLNSRC
CLNACC