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rs1136688

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1136688(A;A)
Make rs1136688(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942984
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1136688
ebirs1136688
HLIrs1136688
Exacrs1136688
Varsomers1136688
Maprs1136688
PheGenIrs1136688
hapmaprs1136688
1000 genomesrs1136688
hgdprs1136688
ensemblrs1136688
gopubmedrs1136688
geneviewrs1136688
scholarrs1136688
googlers1136688
pharmgkbrs1136688
gwascentralrs1136688
openSNPrs1136688
23andMers1136688
23andMe allrs1136688
SNP Nexus

SNPshotrs1136688
SNPdbers1136688
MSV3drs1136688
GWAS Ctlgrs1136688
GMAF0.2893
Max Magnitude0
ClinVar
Risk rs1136688(A,C;A,C)
Alt rs1136688(A,C;A,C)
Reference rs1136688(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910761G; NC_000006.11:g.29910761G>A; NC_000006.11:g.29910761G>C
CLNSRC
CLNACC


GET Evidence
HLA-A-D101N
aa_change Asp101Asn
aa_change_short D101N
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.29787
summary