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rs1136700

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1136700(C;C)
Make rs1136700(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943309
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1136700
ebirs1136700
HLIrs1136700
Exacrs1136700
Varsomers1136700
Maprs1136700
PheGenIrs1136700
hapmaprs1136700
1000 genomesrs1136700
hgdprs1136700
ensemblrs1136700
gopubmedrs1136700
geneviewrs1136700
scholarrs1136700
googlers1136700
pharmgkbrs1136700
gwascentralrs1136700
openSNPrs1136700
23andMers1136700
23andMe allrs1136700
SNP Nexus

SNPshotrs1136700
SNPdbers1136700
MSV3drs1136700
GWAS Ctlgrs1136700
GMAF0.2686
Max Magnitude0
ClinVar
Risk rs1136700(A,C;A,C)
Alt rs1136700(A,C;A,C)
Reference rs1136700(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911086T; NC_000006.11:g.29911086T>A; NC_000006.11:g.29911086T>C
CLNSRC
CLNACC


GET Evidence
HLA-A-S129P
aa_change Ser129Pro
aa_change_short S129P
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.321601
summary