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rs61759956

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61759956(A;A)
Make rs61759956(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942813
GeneHLA-A
is asnp
is mentioned by
dbSNPrs61759956
ebirs61759956
HLIrs61759956
Exacrs61759956
Varsomers61759956
Maprs61759956
PheGenIrs61759956
hapmaprs61759956
1000 genomesrs61759956
hgdprs61759956
ensemblrs61759956
gopubmedrs61759956
geneviewrs61759956
scholarrs61759956
googlers61759956
pharmgkbrs61759956
gwascentralrs61759956
openSNPrs61759956
23andMers61759956
23andMe allrs61759956
SNP Nexus

SNPshotrs61759956
SNPdbers61759956
MSV3drs61759956
GWAS Ctlgrs61759956
Max Magnitude0
ClinVar
Risk rs61759956(A,T;A,T)
Alt rs61759956(A,T;A,T)
Reference rs61759956(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910590C>A; NC_000006.11:g.29910590C>T
CLNSRC
CLNACC