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rs61759958

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61759958(C;G)
Make rs61759958(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942938
GeneHLA-A
is asnp
is mentioned by
dbSNPrs61759958
ebirs61759958
HLIrs61759958
Exacrs61759958
Varsomers61759958
Maprs61759958
PheGenIrs61759958
hapmaprs61759958
1000 genomesrs61759958
hgdprs61759958
ensemblrs61759958
gopubmedrs61759958
geneviewrs61759958
scholarrs61759958
googlers61759958
pharmgkbrs61759958
gwascentralrs61759958
openSNPrs61759958
23andMers61759958
23andMe allrs61759958
SNP Nexus

SNPshotrs61759958
SNPdbers61759958
MSV3drs61759958
GWAS Ctlgrs61759958
Max Magnitude0
ClinVar
Risk rs61759958(A,G,T;A,G,T)
Alt rs61759958(A,G,T;A,G,T)
Reference rs61759958(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910715C>A; NC_000006.11:g.29910715C>G; NC_000006.11:g.29910715C>T
CLNSRC
CLNACC