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rs1136657

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1136657(C;T)
Make rs1136657(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942761
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1136657
ebirs1136657
HLIrs1136657
Exacrs1136657
Varsomers1136657
Maprs1136657
PheGenIrs1136657
hapmaprs1136657
1000 genomesrs1136657
hgdprs1136657
ensemblrs1136657
gopubmedrs1136657
geneviewrs1136657
scholarrs1136657
googlers1136657
pharmgkbrs1136657
gwascentralrs1136657
openSNPrs1136657
23andMers1136657
23andMe allrs1136657
SNP Nexus

SNPshotrs1136657
SNPdbers1136657
MSV3drs1136657
GWAS Ctlgrs1136657
GMAF0.2475
Max Magnitude0
ClinVar
Risk rs1136657(T;T)
Alt rs1136657(T;T)
Reference rs1136657(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910538C>T
CLNSRC
CLNACC