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rs1136697

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1136697(A;T)
Make rs1136697(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943292
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1136697
ebirs1136697
HLIrs1136697
Exacrs1136697
Varsomers1136697
Maprs1136697
PheGenIrs1136697
hapmaprs1136697
1000 genomesrs1136697
hgdprs1136697
ensemblrs1136697
gopubmedrs1136697
geneviewrs1136697
scholarrs1136697
googlers1136697
pharmgkbrs1136697
gwascentralrs1136697
openSNPrs1136697
23andMers1136697
23andMe allrs1136697
SNP Nexus

SNPshotrs1136697
SNPdbers1136697
MSV3drs1136697
GWAS Ctlgrs1136697
GMAF0.157
Max Magnitude0
ClinVar
Risk rs1136697(C,G,T;C,G,T)
Alt rs1136697(C,G,T;C,G,T)
Reference rs1136697(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911069A>C; NC_000006.11:g.29911069A>G; NC_000006.11:g.29911069A>T
CLNSRC
CLNACC


GET Evidence
HLA-A-Y123C
aa_change Tyr123Cys
aa_change_short Y123C
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.00862069
summary