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rs1136689

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1136689(C;C)
Make rs1136689(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942990
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1136689
dbSNP (classic)rs1136689
ClinGenrs1136689
ebirs1136689
HLIrs1136689
Exacrs1136689
Gnomadrs1136689
Varsomers1136689
LitVarrs1136689
Maprs1136689
PheGenIrs1136689
Biobankrs1136689
1000 genomesrs1136689
hgdprs1136689
ensemblrs1136689
geneviewrs1136689
scholarrs1136689
googlers1136689
pharmgkbrs1136689
gwascentralrs1136689
openSNPrs1136689
23andMers1136689
SNPshotrs1136689
SNPdbers1136689
MSV3drs1136689
GWAS Ctlgrs1136689
Max Magnitude0
ClinVar
Risk rs1136689(A;A) rs1136689(C;C)
Alt rs1136689(A;A) rs1136689(C;C)
Reference Rs1136689(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910767G>A; NC_000006.11:g.29910767G>C
CLNSRC
CLNACC