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rs1136659

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1136659(A;A)
Make rs1136659(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942780
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1136659
ebirs1136659
HLIrs1136659
Exacrs1136659
Varsomers1136659
Maprs1136659
PheGenIrs1136659
hapmaprs1136659
1000 genomesrs1136659
hgdprs1136659
ensemblrs1136659
gopubmedrs1136659
geneviewrs1136659
scholarrs1136659
googlers1136659
pharmgkbrs1136659
gwascentralrs1136659
openSNPrs1136659
23andMers1136659
23andMe allrs1136659
SNP Nexus

SNPshotrs1136659
SNPdbers1136659
MSV3drs1136659
GWAS Ctlgrs1136659
GMAF0.09504
Max Magnitude0
ClinVar
Risk rs1136659(A,C;A,C)
Alt rs1136659(A,C;A,C)
Reference rs1136659(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910557T>A; NC_000006.11:g.29910557T>C
CLNSRC
CLNACC


GET Evidence
HLA-A-F33T
aa_change Phe33Thr
aa_change_short F33T
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0762712
summary