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rs1136702

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1136702(G;T)
Make rs1136702(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943315
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1136702
ebirs1136702
HLIrs1136702
Exacrs1136702
Varsomers1136702
Maprs1136702
PheGenIrs1136702
hapmaprs1136702
1000 genomesrs1136702
hgdprs1136702
ensemblrs1136702
gopubmedrs1136702
geneviewrs1136702
scholarrs1136702
googlers1136702
pharmgkbrs1136702
gwascentralrs1136702
openSNPrs1136702
23andMers1136702
23andMe allrs1136702
SNP Nexus

SNPshotrs1136702
SNPdbers1136702
MSV3drs1136702
GWAS Ctlgrs1136702
GMAF0.2475
Max Magnitude0
ClinVar
Risk rs1136702(A,C,T;A,C,T)
Alt rs1136702(A,C,T;A,C,T)
Reference rs1136702(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911092G>A; NC_000006.11:g.29911092G>C; NC_000006.11:g.29911092G>T
CLNSRC
CLNACC


GET Evidence
HLA-A-G131W
aa_change Gly131Trp
aa_change_short G131W
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.129649
summary