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rs1136741

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1136741(C;G)
Make rs1136741(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944124
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1136741
ebirs1136741
HLIrs1136741
Exacrs1136741
Varsomers1136741
Maprs1136741
PheGenIrs1136741
hapmaprs1136741
1000 genomesrs1136741
hgdprs1136741
ensemblrs1136741
gopubmedrs1136741
geneviewrs1136741
scholarrs1136741
googlers1136741
pharmgkbrs1136741
gwascentralrs1136741
openSNPrs1136741
23andMers1136741
23andMe allrs1136741
SNP Nexus

SNPshotrs1136741
SNPdbers1136741
MSV3drs1136741
GWAS Ctlgrs1136741
Max Magnitude0
ClinVar
Risk rs1136741(A,G;A,G)
Alt rs1136741(A,G;A,G)
Reference rs1136741(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911901C>A; NC_000006.11:g.29911901C>G
CLNSRC
CLNACC


GET Evidence
HLA-A-P208A
aa_change Pro208Ala
aa_change_short P208A
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.111111
summary