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rs61759957

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61759957(G;T)
Make rs61759957(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942900
GeneHLA-A
is asnp
is mentioned by
dbSNPrs61759957
ebirs61759957
HLIrs61759957
Exacrs61759957
Varsomers61759957
Maprs61759957
PheGenIrs61759957
hapmaprs61759957
1000 genomesrs61759957
hgdprs61759957
ensemblrs61759957
gopubmedrs61759957
geneviewrs61759957
scholarrs61759957
googlers61759957
pharmgkbrs61759957
gwascentralrs61759957
openSNPrs61759957
23andMers61759957
23andMe allrs61759957
SNP Nexus

SNPshotrs61759957
SNPdbers61759957
MSV3drs61759957
GWAS Ctlgrs61759957
Max Magnitude0
ClinVar
Risk rs61759957(T;T)
Alt rs61759957(T;T)
Reference rs61759957(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910677G>T
CLNSRC
CLNACC