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rs1136692

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1136692(A;A)
Make rs1136692(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943024
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1136692
ebirs1136692
HLIrs1136692
Exacrs1136692
Varsomers1136692
Maprs1136692
PheGenIrs1136692
hapmaprs1136692
1000 genomesrs1136692
hgdprs1136692
ensemblrs1136692
gopubmedrs1136692
geneviewrs1136692
scholarrs1136692
googlers1136692
pharmgkbrs1136692
gwascentralrs1136692
openSNPrs1136692
23andMers1136692
23andMe allrs1136692
SNP Nexus

SNPshotrs1136692
SNPdbers1136692
MSV3drs1136692
GWAS Ctlgrs1136692
GMAF0.2355
Max Magnitude0
ClinVar
Risk rs1136692(A,G;A,G)
Alt rs1136692(A,G;A,G)
Reference rs1136692(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910801C; NC_000006.11:g.29910801C>A; NC_000006.11:g.29910801C>G
CLNSRC
CLNACC


GET Evidence
HLA-A-A114D
aa_change Ala114Asp
aa_change_short A114D
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.255359
summary