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rs1136683

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1136683(C;C)
Make rs1136683(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942975
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1136683
ebirs1136683
HLIrs1136683
Exacrs1136683
Varsomers1136683
Maprs1136683
PheGenIrs1136683
hapmaprs1136683
1000 genomesrs1136683
hgdprs1136683
ensemblrs1136683
gopubmedrs1136683
geneviewrs1136683
scholarrs1136683
googlers1136683
pharmgkbrs1136683
gwascentralrs1136683
openSNPrs1136683
23andMers1136683
23andMe allrs1136683
SNP Nexus

SNPshotrs1136683
SNPdbers1136683
MSV3drs1136683
GWAS Ctlgrs1136683
GMAF0.2782
Max Magnitude0
ClinVar
Risk rs1136683(A,C;A,C)
Alt rs1136683(A,C;A,C)
Reference rs1136683(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910752G>A; NC_000006.11:g.29910752G>C
CLNSRC
CLNACC


GET Evidence
HLA-A-D98H
aa_change Asp98His
aa_change_short D98H
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.225815
summary