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rs1136690

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1136690(C;T)
Make rs1136690(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942994
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1136690
ebirs1136690
HLIrs1136690
Exacrs1136690
Varsomers1136690
Maprs1136690
PheGenIrs1136690
hapmaprs1136690
1000 genomesrs1136690
hgdprs1136690
ensemblrs1136690
gopubmedrs1136690
geneviewrs1136690
scholarrs1136690
googlers1136690
pharmgkbrs1136690
gwascentralrs1136690
openSNPrs1136690
23andMers1136690
23andMe allrs1136690
SNP Nexus

SNPshotrs1136690
SNPdbers1136690
MSV3drs1136690
GWAS Ctlgrs1136690
Max Magnitude0
ClinVar
Risk rs1136690(A,T;A,T)
Alt rs1136690(A,T;A,T)
Reference rs1136690(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910771C>A; NC_000006.11:g.29910771C>T
CLNSRC
CLNACC